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5.44 Organometallic Chemistry (MIT) 5.44 Organometallic Chemistry (MIT)

Description

This course examines important transformations of organotransition-metal species with an emphasis on basic mechanisms, structure-reactivity relationships, and applications in organic synthesis. This course examines important transformations of organotransition-metal species with an emphasis on basic mechanisms, structure-reactivity relationships, and applications in organic synthesis.

Subjects

organometallic chemistry | organometallic chemistry | formal charge | formal charge | oxidation state | oxidation state | d electron count | d electron count | hapticity | hapticity | coordination number | coordination number | ligands | ligands | 18-electron rule | 18-electron rule | ligand substitution reaction | ligand substitution reaction | oxidative addition | oxidative addition | reductive elimination | reductive elimination | migratory insertion | migratory insertion | reductive coupling | reductive coupling | cycloaddition | cycloaddition

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5.512 Synthetic Organic Chemistry II (MIT) 5.512 Synthetic Organic Chemistry II (MIT)

Description

This course focuses on general methods and strategies for the synthesis of complex organic molecules. Emphasis is on strategies for stereoselective synthesis, including stereocontrolled synthesis of complex acyclic compounds. This course focuses on general methods and strategies for the synthesis of complex organic molecules. Emphasis is on strategies for stereoselective synthesis, including stereocontrolled synthesis of complex acyclic compounds.

Subjects

synthetic organic chemistry | synthetic organic chemistry | synthesis | synthesis | complex organic molecules | complex organic molecules | stereoselective synthesis | stereoselective synthesis | acyclic compounds | acyclic compounds | stereocontrolled synthesis | stereocontrolled synthesis | stereocontrolled alkylation | stereocontrolled alkylation | stereocontrolled conjugate addition | stereocontrolled conjugate addition | carbonyls | carbonyls | aldol reactions | aldol reactions | carbonyl reduction | carbonyl reduction | alkene reduction | alkene reduction | hydroboration | hydroboration | dihydroxylation | dihydroxylation | epoxidation | epoxidation

License

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5.05 Principles of Inorganic Chemistry III (MIT) 5.05 Principles of Inorganic Chemistry III (MIT)

Description

This course covers the principles of main group (s and p block) element chemistry with an emphasis on synthesis, structure, bonding, and reaction mechanisms. This course covers the principles of main group (s and p block) element chemistry with an emphasis on synthesis, structure, bonding, and reaction mechanisms.

Subjects

inorganic chemistry | inorganic chemistry | main group element chemistry | main group element chemistry | chemical synthesis | chemical synthesis | chemical structure | chemical structure | bonding | bonding | reaction mechanisms | reaction mechanisms | aluminum chemistry | aluminum chemistry | s block | s block | p block | p block | interatomic distance | interatomic distance | lewis structure | lewis structure | partitions space | partitions space | Density Functional Theory | Density Functional Theory | NMR spectroscopy | NMR spectroscopy | spin-orbit coupling | spin-orbit coupling | spin-spin coupling | spin-spin coupling | relativistic effects | relativistic effects | spin-orbit effects | spin-orbit effects | noble gas chemistry | noble gas chemistry | chemical reaction products | chemical reaction products

License

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5.08J Biological Chemistry II (MIT) 5.08J Biological Chemistry II (MIT)

Description

This course deals with a more advanced treatment of the biochemical mechanisms that underlie biological processes. Emphasis will be given to the experimental methods used to unravel how these processes fit into the cellular context as well as the coordinated regulation of these processes. Topics include macromolecular machines for energy and force transduction, regulation of biosynthetic and degradative pathways, and the structure and function of nucleic acids. This course deals with a more advanced treatment of the biochemical mechanisms that underlie biological processes. Emphasis will be given to the experimental methods used to unravel how these processes fit into the cellular context as well as the coordinated regulation of these processes. Topics include macromolecular machines for energy and force transduction, regulation of biosynthetic and degradative pathways, and the structure and function of nucleic acids.

Subjects

biochemistry | biochemistry | biological chemistry | biological chemistry | Rasmol | Rasmol | Deep Viewer | Deep Viewer | CHIME | CHIME | BLAST | BLAST | PDB | PDB | macromolecular machines | macromolecular machines | protein folding | protein folding | protein degradation | protein degradation | fatty acid synthases | fatty acid synthases | polyketide synthases | polyketide synthases | non-ribosomal polypeptide synthases | non-ribosomal polypeptide synthases | metal homeostasis | metal homeostasis | biochemical mechanisms | biochemical mechanisms | biochemical pathways | biochemical pathways | macromolecular interactions | macromolecular interactions | ribosome | ribosome | mRNA | mRNA | metabolic networking | metabolic networking | 5.08 | 5.08 | 7.08 | 7.08

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12.335 Experimental Atmospheric Chemistry (MIT) 12.335 Experimental Atmospheric Chemistry (MIT)

Description

This course provides an introduction to the atmospheric chemistry involved in climate change, air pollution and biogeochemical cycles using a combination of hands-on laboratory, field studies, and simple computer models. Lectures will be accompanied by field trips to collect air samples for the analysis of gases, aerosols and clouds by the students. This course provides an introduction to the atmospheric chemistry involved in climate change, air pollution and biogeochemical cycles using a combination of hands-on laboratory, field studies, and simple computer models. Lectures will be accompanied by field trips to collect air samples for the analysis of gases, aerosols and clouds by the students.

Subjects

atmospheric chemistry | atmospheric chemistry | climate change | climate change | air pollution | air pollution | urban environment | urban environment | biogeochemical cycles | biogeochemical cycles | gases | gases | aerosols | aerosols | precipitation | precipitation | photochemistry | photochemistry

License

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5.04 Principles of Inorganic Chemistry II (MIT) 5.04 Principles of Inorganic Chemistry II (MIT)

Description

This course provides a systematic presentation of the chemical applications of group theory with emphasis on the formal development of the subject and its applications to the physical methods of inorganic chemical compounds. The electronic structure of molecules will be developed. Against this backdrop, the optical, vibrational, and magnetic properties of transition metal complexes are presented and their investigation by the appropriate spectroscopy is described. This course provides a systematic presentation of the chemical applications of group theory with emphasis on the formal development of the subject and its applications to the physical methods of inorganic chemical compounds. The electronic structure of molecules will be developed. Against this backdrop, the optical, vibrational, and magnetic properties of transition metal complexes are presented and their investigation by the appropriate spectroscopy is described.

Subjects

inorganic chemistry | inorganic chemistry | group theory | group theory | transition metal complexes | transition metal complexes | symmetry element | symmetry element | point group | point group | LCAO | LCAO | metal metal bonding | metal metal bonding | vibrational spectroscopy | vibrational spectroscopy | character tables | character tables | sandwich compounds | sandwich compounds

License

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5.13 Organic Chemistry II (MIT) 5.13 Organic Chemistry II (MIT)

Description

This intermediate organic chemistry course focuses on the methods used to identify the structure of organic molecules, advanced principles of organic stereochemistry, organic reaction mechanisms, and methods used for the synthesis of organic compounds. Additional special topics include illustrating the role of organic chemistry in biology, medicine, and industry. This intermediate organic chemistry course focuses on the methods used to identify the structure of organic molecules, advanced principles of organic stereochemistry, organic reaction mechanisms, and methods used for the synthesis of organic compounds. Additional special topics include illustrating the role of organic chemistry in biology, medicine, and industry.

Subjects

intermediate organic chemistry | intermediate organic chemistry | organic molecules | organic molecules | stereochemistry | stereochemistry | reaction mechanisms | reaction mechanisms | synthesis of organic compounds | synthesis of organic compounds | synthesis | synthesis | structure determination | structure determination | mechanism | mechanism | reactivity | reactivity | functional groups | functional groups | NMR | NMR | spectroscopy | spectroscopy | spectrometry | spectrometry | structure elucidation | structure elucidation | infrared spectroscopy | infrared spectroscopy | nuclear magnetic resonance spectroscopy | nuclear magnetic resonance spectroscopy | reactive intermediates | reactive intermediates | carbocations | carbocations | radicals | radicals | aromaticity | aromaticity | conjugated systems | conjugated systems | molecular orbital theory | molecular orbital theory | pericyclic reactions | pericyclic reactions

License

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5.12 Organic Chemistry I (MIT) 5.12 Organic Chemistry I (MIT)

Description

5.12 is an introduction to organic chemistry, focusing primarily on the basic principles to understand the structure and reactivity of organic molecules. Emphasis is on substitution and elimination reactions and chemistry of the carbonyl group. The course also provides an introduction to the chemistry of aromatic compounds. 5.12 is an introduction to organic chemistry, focusing primarily on the basic principles to understand the structure and reactivity of organic molecules. Emphasis is on substitution and elimination reactions and chemistry of the carbonyl group. The course also provides an introduction to the chemistry of aromatic compounds.

Subjects

organic chemistry | organic chemistry | structure | structure | reactivity | reactivity | organic molecules | organic molecules | substitution | substitution | carbonyl group | carbonyl group | elimination | elimination

License

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5.13 Organic Chemistry II (MIT) 5.13 Organic Chemistry II (MIT)

Description

5.13 is an intermediate organic chemistry course that deals primarily with synthesis, structure determination, mechanism, and the relationships between structure and reactivity emphasized. Special topics in organic chemistry are included to illustrate the role of organic chemistry in biological systems, medicine, and in the chemical industry. 5.13 is an intermediate organic chemistry course that deals primarily with synthesis, structure determination, mechanism, and the relationships between structure and reactivity emphasized. Special topics in organic chemistry are included to illustrate the role of organic chemistry in biological systems, medicine, and in the chemical industry.

Subjects

intermediate organic chemistry | intermediate organic chemistry | organic | organic | organic molecules | organic molecules | stereochemistry | stereochemistry | reaction mechanisms | reaction mechanisms | synthesis of organic compounds | synthesis of organic compounds | synthesis | synthesis | structure determination | structure determination | mechanism | mechanism | structure | structure | reactivity | reactivity

License

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12.301 Past and Present Climate (12.301) / Climate Physics and Chemistry (12.842) (MIT) 12.301 Past and Present Climate (12.301) / Climate Physics and Chemistry (12.842) (MIT)

Description

This course introduces students to climate studies, including beginnings of the solar system, time scales, and climate in human history. This course introduces students to climate studies, including beginnings of the solar system, time scales, and climate in human history.

Subjects

climate | climate | climate change | climate change | proxies | proxies | ice cores | ice cores | primordial atmosphere | primordial atmosphere | ozone chemistry | ozone chemistry | carbon and oxygen cycles | carbon and oxygen cycles | heat and water budgets | heat and water budgets | aerosols | aerosols | water vapor | water vapor | clouds | clouds | ocean circulation | ocean circulation | orbital variations | orbital variations | volcanism | volcanism | plate tectonics | plate tectonics | solar system | solar system | solar variability | solar variability | climate model | climate model | energy balance | energy balance

License

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SP.287 Kitchen Chemistry (MIT) SP.287 Kitchen Chemistry (MIT)

Description

This seminar is designed to be an experimental and hands-on approach to applied chemistry (as seen in cooking). Cooking may be the oldest and most widespread application of chemistry and recipes may be the oldest practical result of chemical research. We shall do some cooking experiments to illustrate some chemical principles, including extraction, denaturation, and phase changes. This seminar is designed to be an experimental and hands-on approach to applied chemistry (as seen in cooking). Cooking may be the oldest and most widespread application of chemistry and recipes may be the oldest practical result of chemical research. We shall do some cooking experiments to illustrate some chemical principles, including extraction, denaturation, and phase changes.

Subjects

cooking | cooking | food | food | chemistry | chemistry | cook | cook | edible | edible | kitchen | kitchen

License

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UC Irvine OpenCourseWare: Interview with Professor James Nowick

Description

James S. Nowick was born in 1964 and received his A.B. degree from Columbia University in 1985. He was both an NSF Graduate Fellow and an ACS Division of Organic Chemistry Graduate Fellow during his graduate studies at MIT, where he earned his Ph.D. degree in 1990 under the supervision of Rick L. Danheiser. After an NSF postdoctoral fellowship with Professor Julius Rebek at MIT, he began his independent career as an Assistant Professor at the University of California, Irvine (UCI) in 1991. He was promoted to Associate Professor in 1996 and Professor in 1998. Professor Nowick's research interests include peptidomimetic chemistry, molecular recognition, and bioorganic catalysis. He is committed to chemical education and runs the UCI Chemistry Outreach Program, which reaches over 2000 high school students each year. Professor Nowick received a Camille and Henry Dreyfus Foundation New Faculty Award (1991), an American Cancer Society Junior Faculty Research Award (1992), an NSF Young Investigator Award (1992), an Arnold and Mabel Beckman Foundation Young Investigator Award (1994), a Presidential Faculty Fellow Award (1995), a Camille Dreyfus Teacher-Scholar Award (1996), an Alfred P. Sloan Research Fellowship (1997), and an American Chemical Society Arthur C. Cope Scholar Award (1998). For his contributions to undergraduate education at UCI, he has received the UCI Award for Outstanding Faculty Contributions to Undergraduate Research (1995), the Chancellor's Award for Excellence in Undergraduate Research (1997) and the UCI School of Physical Sciences Award for Outstanding Contributions to Undergraduate Education (1999). As a proud member of the OCW Consortium, the University of California, Irvine strives to play a significant role in the contribution to the social welfare of the state, the nation and the world by making high quality UC course materials free on a global scale to educators, students, and self-learners. For more information, please visit our official home page at: http://ocw.uci.edu

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5.36 Biochemistry Laboratory (MIT)

Description

The course, which spans two thirds of a semester, provides students with a research-inspired laboratory experience that introduces standard biochemical techniques in the context of investigating a current and exciting research topic, acquired resistance to the cancer drug Gleevec. Techniques include protein expression, purification, and gel analysis, PCR, site-directed mutagenesis, kinase activity assays, and protein structure viewing. This class is part of the new laboratory curriculum in the MIT Department of Chemistry. Undergraduate Research-Inspired Experimental Chemistry Alternatives (URIECA) introduces students to cutting edge research topics in a modular format. Acknowledgments Development of this course was funded through an HHMI Professors grant to Professor Catherine L. Drennan.

Subjects

URIECA | laboratory | kinase | cancer cells | laboratory techniques | DNA | cultures | UV-Vis | agarose gel | Abl-gleevec | affinity tags | lyse | digest | mutants | resistance | gel electrophoresis | recombinant | nickel affinity | inhibitors | biochemistry | kinetics | enzyme | inhibition | purification | expression

License

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The molecular world The molecular world

Description

From diamonds to dynamite, everything involves a chemical reaction. This free course, The molecular world, introduces you to the concepts and principles that underpin chemistry at the molecular level. Everyday experiences are used to help you to understand the more complex issues. First published on Tue, 22 Mar 2016 as The molecular world. To find out more visit The Open University's Openlearn website. Creative-Commons 2016 From diamonds to dynamite, everything involves a chemical reaction. This free course, The molecular world, introduces you to the concepts and principles that underpin chemistry at the molecular level. Everyday experiences are used to help you to understand the more complex issues. First published on Tue, 22 Mar 2016 as The molecular world. To find out more visit The Open University's Openlearn website. Creative-Commons 2016

Subjects

Chemistry | Chemistry | nucleus | nucleus | protons | protons | periodic table | periodic table | metals | metals | S205_2 | S205_2

License

Except for third party materials and otherwise stated (see http://www.open.ac.uk/conditions terms and conditions), this content is made available under a http://creativecommons.org/licenses/by-nc-sa/2.0/uk/ Creative Commons Attribution-NonCommercial-ShareAlike 2.0 Licence Licensed under a Creative Commons Attribution - NonCommercial-ShareAlike 2.0 Licence - see http://creativecommons.org/licenses/by-nc-sa/2.0/uk/ - Original copyright The Open University

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5.310 Laboratory Chemistry (MIT)

Description

Laboratory Chemistry (5.310) introduces experimental chemistry for students requiring a chemistry laboratory who are not majoring in chemistry. Students must have completed general chemistry (5.111) and have completed or be concurrently enrolled in the first semester of organic chemistry (5.12). The course covers principles and applications of chemical laboratory techniques, including preparation and analysis of chemical materials, measurement of pH, gas and liquid chromatography, visible-ultraviolet spectrophotometry, infrared spectroscopy, kinetics, data analysis, and elementary synthesis. NOTE: The Staff for this course would like to acknowledge that the experiments include contributions from past instructors, course textbooks, and others affiliated with course #5.310. Since the

Subjects

lab | chemistry | laboratory | experiment | pH | gas chromatography | liquid chromatography | visible-ultraviolet spectrophotometry | infrared spectroscopy | kinetics | data analysis | elementary synthesis | amino acid | ferrocene | essential oil | potentiometric titration | techniques | measurement | materials | data | analysis | elementary | synthesis | amino | acid | essential | oil | gas | chromatography | infrared | spectroscopy | liquid | potentiometric | titration | visible | ultraviolet | spectrophotometry

License

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5.310 Laboratory Chemistry (MIT)

Description

Laboratory Chemistry (5.310) introduces experimental chemistry for students requiring a chemistry laboratory who are not majoring in chemistry. Students must have completed general chemistry (5.111) and have completed or be concurrently enrolled in the first semester of organic chemistry (5.12). The course covers principles and applications of chemical laboratory techniques, including preparation and analysis of chemical materials, measurement of pH, gas and liquid chromatography, visible-ultraviolet spectrophotometry, infrared spectroscopy, kinetics, data analysis, and elementary synthesis. NOTE: The Staff for this course would like to acknowledge that the experiments include contributions from past instructors, course textbooks, and others affiliated with course #5.310. Since the

Subjects

lab | chemistry | laboratory | experiment | pH | gas chromatography | liquid chromatography | visible-ultraviolet spectrophotometry | infrared spectroscopy | kinetics | data analysis | elementary synthesis | amino acid | ferrocene | essential oil | potentiometric titration | techniques | measurement | materials | data | analysis | elementary | synthesis | amino | acid | essential | oil | gas | chromatography | infrared | spectroscopy | liquid | potentiometric | titration | visible | ultraviolet | spectrophotometry

License

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ES.SP.287 Kitchen Chemistry (MIT) ES.SP.287 Kitchen Chemistry (MIT)

Description

This seminar is designed to be an experimental and hands-on approach to applied chemistry (as seen in cooking). Cooking may be the oldest and most widespread application of chemistry and recipes may be the oldest practical result of chemical research. We shall do some cooking experiments to illustrate some chemical principles, including extraction, denaturation, and phase changes. This seminar is designed to be an experimental and hands-on approach to applied chemistry (as seen in cooking). Cooking may be the oldest and most widespread application of chemistry and recipes may be the oldest practical result of chemical research. We shall do some cooking experiments to illustrate some chemical principles, including extraction, denaturation, and phase changes.

Subjects

cooking | cooking | food | food | chemistry | chemistry | experiment | experiment | extraction | extraction | denaturation | denaturation | phase change | phase change | capsicum | capsicum | biochemistry | biochemistry | chocolate | chocolate | cheese | cheese | yeast | yeast | recipe | recipe | jam | jam | pectin | pectin | enzyme | enzyme | dairy | dairy | molecular gastronomy | molecular gastronomy | salt | salt | colloid | colloid | stability | stability | liquid nitrogen | liquid nitrogen | ice cream | ice cream | biology | biology | microbiology | microbiology

License

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5.62 Physical Chemistry II (MIT)

Description

This subject deals primarily with elementary statistical mechanics, transport properties, kinetic theory, solid state, reaction rate theory, and chemical reaction dynamics.AcknowledgementsThe lecture note materials for this course include contributions from Professor Sylvia T. Ceyer. The Staff for this course would like to acknowledge that these course materials include contributions from past instructors, textbooks, and other members of the MIT Chemistry Department affiliated with course #5.62. Since the following works have evolved over a period of many years, no single source can be attributed.

Subjects

physical chemistry | partition functions | atomic degrees of freedom | molecular degrees of freedom | chemical equilibrium | thermodynamics | intermolecular potentials | equations of state | solid state chemistry | einstein and debye solids | kinetic theory | rate theory | chemical kinetics | transition state theory | RRKM theory | collision theory | equipartition | fermi-dirac statistics | boltzmann statistics | bose-einstein statistics | statistical mechanics

License

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5.62 Physical Chemistry II (MIT)

Description

This course covers elementary statistical mechanics, transport properties, kinetic theory, solid state, reaction rate theory, and chemical reaction dynamics. Acknowledgements The staff for this course would like to acknowledge that these course materials include contributions from past instructors, textbooks, and other members of the MIT Chemistry Department affiliated with course #5.62. Since the following works have evolved over a period of many years, no single source can be attributed.

Subjects

physical chemistry | partition functions | atomic degrees of freedom | molecular degrees of freedom | chemical equilibrium | thermodynamics | intermolecular potentials | equations of state | solid state chemistry | einstein and debye solids | kinetic theory | rate theory | chemical kinetics | transition state theory | RRKM theory | collision theory | equipartition | fermi-dirac statistics | boltzmann statistics | bose-einstein statistics | statistical mechanics

License

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SP.235 Chemistry of Sports (MIT) SP.235 Chemistry of Sports (MIT)

Description

Subjects

organs | organs | cardiovascular | cardiovascular | muscles | muscles | training | training | nutrition | nutrition | fueling | fueling | repair | repair | maintenance | maintenance | swimming | swimming | running | running | cycling | cycling | bicycle | bicycle | bike | bike | shoes | shoes | sports drinks | sports drinks | caffeine | caffeine | alcohol | alcohol | exercise | exercise | competition | competition | endurance | endurance | strength | strength | EPO | EPO | erythropoietin | erythropoietin | scandals | scandals | tapering | tapering | triathlon | triathlon | sports | sports | race | race | steroids | steroids

License

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Chem 201. Organic Reaction Mechanisms I. Lecture 19. Sulfur Chemistry

Description

UCI Chem 201 Organic Reaction Mechanisms I (Fall 2012) Lec 19. Organic Reaction Mechanism -- Sulfur Chemistry View the complete course: http://ocw.uci.edu/courses/chem_201_organic_reactions_mechanisms_i.html Instructor: David Van Vranken, Ph.D. License: Creative Commons BY-NC-SA Terms of Use: http://ocw.uci.edu/info. More courses at http://ocw.uci.edu Description: Advanced treatment of basic mechanistic principles of modern organic chemistry. Topics include molecular orbital theory, orbital symmetry control of organic reactions, aromaticity, carbonium ion chemistry, free radical chemistry, the chemistry of carbenes and carbanions, photochemistry, electrophilic substitutions, aromatic chemistry. Organic Reaction Mechanisms I (Chem 201) is part of OpenChem: http://ocw.uci.edu/collections/open_chemistry.html This video is part of a 20-lecture graduate-level course titled "Organic Reaction Mechanisms I" taught at UC Irvine by Professor David Van Vranken. Recorded December 5, 2012. Required attribution: Van Vranken, David Organic Reaction Mechanisms 201 (UCI OpenCourseWare: University of California, Irvine), http://ocw.uci.edu/courses/chem_201_organic_reactions_mechanisms_i.html [Access date]. License: Creative Commons Attribution-ShareAlike 3.0 United States License.

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The Zeroth Law of Thermodynamics and Temperature

Description

In this video I shall present the context for the creation of the 0th Law of Thermodynamics. And describe how it renewed confidence in our ability to measure temperature. This context will involve a very brief description of the first three laws of thermodynamics.

Subjects

chemistry | University of Manchester | Faculty of Engineering and Physical Sciences | School of Chemistry | physical chemistry | Quantum Chemistry | virtual lab | virtual experiment | Physical Sciences

License

Attribution-NonCommercial-ShareAlike 4.0 International Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ http://creativecommons.org/licenses/by-nc-sa/4.0/

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7.012 Introduction to Biology (MIT) 7.012 Introduction to Biology (MIT)

Description

All three courses: 7.012, 7.013 and 7.014 cover the same core material which includes: the fundamental principles of biochemistry as they apply to introductory biology, genetics, molecular biology, basic recombinant DNA technology, and gene regulation.In addition, each version of the subject has its own distinctive material, described below. Note: All three versions require a familiarity with some basic chemistry. For details, see the Chemistry Self-evaluation.7.012 focuses on cell biology, immunology, neurobiology, and includes an exploration into current research in cancer, genomics, and molecular medicine. 7.013 focuses on the application of the fundamental principles toward an understanding of cells, human genetics and diseases, infectious agents, cancer, immunology, molecular All three courses: 7.012, 7.013 and 7.014 cover the same core material which includes: the fundamental principles of biochemistry as they apply to introductory biology, genetics, molecular biology, basic recombinant DNA technology, and gene regulation.In addition, each version of the subject has its own distinctive material, described below. Note: All three versions require a familiarity with some basic chemistry. For details, see the Chemistry Self-evaluation.7.012 focuses on cell biology, immunology, neurobiology, and includes an exploration into current research in cancer, genomics, and molecular medicine. 7.013 focuses on the application of the fundamental principles toward an understanding of cells, human genetics and diseases, infectious agents, cancer, immunology, molecular

Subjects

amino acids | amino acids | biochemistry | biochemistry | cancer | cancer | cell biology | cell biology | cell cycle | cell cycle | cell signaling | cell signaling | cloning | cloning | DNA | DNA | endoplasmic reticulum | endoplasmic reticulum | gene regulation | gene regulation | gene structure | gene structure | genetics | genetics | genomics | genomics | immunology | immunology | molecular biology | molecular biology | molecular medicine | molecular medicine | mRNA | mRNA | nervous system | nervous system | neurobiology | neurobiology | PCR | PCR | polymerase chain reaction | polymerase chain reaction | polypeptide chain | polypeptide chain | protein localization | protein localization | protein structure | protein structure | protein synthesis | protein synthesis | proteins | proteins | recombinant DNA | recombinant DNA | replication | replication | ribosome | ribosome | RNA | RNA | stem cells | stem cells | transcription | transcription | translation | translation | virology | virology | biology | biology

License

Content within individual OCW courses is (c) by the individual authors unless otherwise noted. MIT OpenCourseWare materials are licensed by the Massachusetts Institute of Technology under a Creative Commons License (Attribution-NonCommercial-ShareAlike). For further information see http://ocw.mit.edu/terms/index.htm

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What chemical compounds might be present in drinking water? What chemical compounds might be present in drinking water?

Description

Do you want to know whats in the water that you drink? This free course, What chemical compounds might be present in drinking water?, examines the chemical compounds that occur in drinking water. A high level of certain anions in water can cause environmental pollution and health problems. Cations are also important. For example, calcium salts contribute to the hardness of water and water treatment uses aluminium compounds. Additionally oxidising agents, such as ozone or chlorine, are vital in the disinfection of water. This OpenLearn course focuses on the chemistry of the p-block elements in Groups 13 to 18 of the Periodic Table. First published on Mon, 21 Mar 2016 as What chemical compounds might be present in drinking water?. To find out more visit The Open University's Openlearn websi Do you want to know whats in the water that you drink? This free course, What chemical compounds might be present in drinking water?, examines the chemical compounds that occur in drinking water. A high level of certain anions in water can cause environmental pollution and health problems. Cations are also important. For example, calcium salts contribute to the hardness of water and water treatment uses aluminium compounds. Additionally oxidising agents, such as ozone or chlorine, are vital in the disinfection of water. This OpenLearn course focuses on the chemistry of the p-block elements in Groups 13 to 18 of the Periodic Table. First published on Mon, 21 Mar 2016 as What chemical compounds might be present in drinking water?. To find out more visit The Open University's Openlearn websi

Subjects

Science | Maths & Technology | Science | Maths & Technology | Science | Science | Chemistry | Chemistry | S215_1 | S215_1 | water | water | ions | ions | nitrogen cycle | nitrogen cycle | arsenic | arsenic | polyprotic | polyprotic | aluminium | aluminium

License

Except for third party materials and otherwise stated (see http://www.open.ac.uk/conditions terms and conditions), this content is made available under a http://creativecommons.org/licenses/by-nc-sa/2.0/uk/ Creative Commons Attribution-NonCommercial-ShareAlike 2.0 Licence Licensed under a Creative Commons Attribution - NonCommercial-ShareAlike 2.0 Licence - see http://creativecommons.org/licenses/by-nc-sa/2.0/uk/ - Original copyright The Open University

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5.301 Chemistry Laboratory Techniques (MIT) 5.301 Chemistry Laboratory Techniques (MIT)

Description

This course is an intensive introduction to the techniques of experimental chemistry and gives first year students an opportunity to learn and master the basic chemistry lab techniques for carrying out experiments. Students who successfully complete the course and obtain a "Competent Chemist" (CC) or "Expert Experimentalist" (EE) rating are likely to secure opportunities for research work in a chemistry lab at MIT. Acknowledgements The laboratory manual and materials for this course were prepared by Dr. Katherine J. Franz and Dr. Kevin M. Shea with the assistance of Professors Rick L. Danheiser and Timothy M. Swager. Materials have been revised by Dr. J. Haseltine, Dr. Kevin M. Shea, and Dr. Sarah A. Tabacco. WARNING NOTICE The experiments described in these materials a This course is an intensive introduction to the techniques of experimental chemistry and gives first year students an opportunity to learn and master the basic chemistry lab techniques for carrying out experiments. Students who successfully complete the course and obtain a "Competent Chemist" (CC) or "Expert Experimentalist" (EE) rating are likely to secure opportunities for research work in a chemistry lab at MIT. Acknowledgements The laboratory manual and materials for this course were prepared by Dr. Katherine J. Franz and Dr. Kevin M. Shea with the assistance of Professors Rick L. Danheiser and Timothy M. Swager. Materials have been revised by Dr. J. Haseltine, Dr. Kevin M. Shea, and Dr. Sarah A. Tabacco. WARNING NOTICE The experiments described in these materials a

Subjects

chemistry | chemistry | experiment | experiment | laboratory techniques | laboratory techniques | purification | purification | transfer and extraction | transfer and extraction | column chromatography | column chromatography | protein assays | protein assays | error analysis | error analysis | NMR | NMR | IR | IR | gas chromatography | gas chromatography | spectroscopy | spectroscopy | UV-Vis | UV-Vis | experimental chemistry | experimental chemistry | original research projects | original research projects

License

Content within individual OCW courses is (c) by the individual authors unless otherwise noted. MIT OpenCourseWare materials are licensed by the Massachusetts Institute of Technology under a Creative Commons License (Attribution-NonCommercial-ShareAlike). For further information see http://ocw.mit.edu/terms/index.htm

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