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Organic Chemistry
Jonathan Clayden, Nick Greeves - ISBN: 9780199270293
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On this page you find summaries, notes, study guides and many more for the textbook Organic Chemistry, written by Jonathan Clayden & Nick Greeves. The summaries are written by students themselves, which gives you the best possible insight into what is important to study about this book. Subjects like Chemistry, answers, biotechnology, peptide chemistry, heterocycles, aromatic chemistry, biology & biomed will be dealt with.
Popular summaries Organic Chemistry Notes
unit 16 assignment which is done up to high standard i have achieved overall DISTINCTION.
- Essay
- • 14 pages •
unit 16 assignment which is done up to high standard i have achieved overall DISTINCTION.
This is a handwritten summary of the course Organic Chemistry at the VU. It concerns chapters 2, 4, 5, 6, 7, 8, 10 and 11. It also contains useful drawings and comments.
- Summary
- • 24 pages •
This is a handwritten summary of the course Organic Chemistry at the VU. It concerns chapters 2, 4, 5, 6, 7, 8, 10 and 11. It also contains useful drawings and comments.
This is summary of : 1. Acids and Bases Chemistry - what causes stability or instability - properties of various acids/bases and stability series - types of acids and bases - interpretation of pKa and pKaH values 2. Organic Chemistry - reaction mechanisms - carbonyl group chemistry (involving keto-enol chemistry, acetals, ketals, hemiacetals, hemiketals, organolithiums / Grignard reagents) - overview of functional groups - stereochemistry
- Summary
- • 24 pages •
This is summary of : 1. Acids and Bases Chemistry - what causes stability or instability - properties of various acids/bases and stability series - types of acids and bases - interpretation of pKa and pKaH values 2. Organic Chemistry - reaction mechanisms - carbonyl group chemistry (involving keto-enol chemistry, acetals, ketals, hemiacetals, hemiketals, organolithiums / Grignard reagents) - overview of functional groups - stereochemistry
I got a 1st in my first year studying chemistry at the University of Birmingham using these revision notes that I have uploaded. They include detail on acidity, electron density and chemical reactivity, drawing reaction mechanisms, nucleophilic substitution reactions: the SN1 and SN2 reaction mechanisms and elimination reactions: the E1 and E2 reaction mechanisms. These summary notes also include worked examples as revision practice.
- Summary
- • 9 pages •
I got a 1st in my first year studying chemistry at the University of Birmingham using these revision notes that I have uploaded. They include detail on acidity, electron density and chemical reactivity, drawing reaction mechanisms, nucleophilic substitution reactions: the SN1 and SN2 reaction mechanisms and elimination reactions: the E1 and E2 reaction mechanisms. These summary notes also include worked examples as revision practice.
I got a 1st in my first year studying chemistry at the University of Birmingham using these revision notes that I have uploaded. They include detail on drawing and naming molecules, structure and bonding in hydrocarbons, conformational analysis and stereochemistry. These summary notes also include worked examples as revision practice.
- Summary
- • 8 pages •
I got a 1st in my first year studying chemistry at the University of Birmingham using these revision notes that I have uploaded. They include detail on drawing and naming molecules, structure and bonding in hydrocarbons, conformational analysis and stereochemistry. These summary notes also include worked examples as revision practice.
Pericyclic reactions. The material covered in this section includes (i) analysis of electrocyclic reactions, (ii) cycloaddition reactions and (iii) sigmatropic rearrangements by both a frontier orbital approach and by application of Woodward-Hoffmann rules.
- Class notes
- • 14 pages •
Pericyclic reactions. The material covered in this section includes (i) analysis of electrocyclic reactions, (ii) cycloaddition reactions and (iii) sigmatropic rearrangements by both a frontier orbital approach and by application of Woodward-Hoffmann rules.
summaries for organic 2 for IR and MS. these summaries includes practice questions and notes from both lectures notes, books, professors notes.
- Summary
- • 9 pages •
summaries for organic 2 for IR and MS. these summaries includes practice questions and notes from both lectures notes, books, professors notes.
Lecture 4 of the Aromatic and Heteroaromatic course at Durham University, hand-written, neat diagrams.
- Class notes
- • 2 pages •
Lecture 4 of the Aromatic and Heteroaromatic course at Durham University, hand-written, neat diagrams.
I got a 1st in my first year studying chemistry at the University of Birmingham using these revision notes that I have uploaded. They include detail on structure of benzene, stability of aromatic compounds, criteria for aromaticity, electrophilic substitution, benzene vs olefin reactivity with electrophiles, arrow-pushing mechanisms for a range of electrophilic aromatic substitution reactions, functional group interconversion, selectivity in substitution reactions, how substitutents on a benzene...
- Summary
- • 7 pages •
I got a 1st in my first year studying chemistry at the University of Birmingham using these revision notes that I have uploaded. They include detail on structure of benzene, stability of aromatic compounds, criteria for aromaticity, electrophilic substitution, benzene vs olefin reactivity with electrophiles, arrow-pushing mechanisms for a range of electrophilic aromatic substitution reactions, functional group interconversion, selectivity in substitution reactions, how substitutents on a benzene...
Includes answers for ALL questions in exam paper
- Exam (elaborations)
- • 10 pages •
Includes answers for ALL questions in exam paper
Latest notes & summaries Organic Chemistry Notes
This is summary of : 1. Acids and Bases Chemistry - what causes stability or instability - properties of various acids/bases and stability series - types of acids and bases - interpretation of pKa and pKaH values 2. Organic Chemistry - reaction mechanisms - carbonyl group chemistry (involving keto-enol chemistry, acetals, ketals, hemiacetals, hemiketals, organolithiums / Grignard reagents) - overview of functional groups - stereochemistry
- Summary
- • 24 pages •
This is summary of : 1. Acids and Bases Chemistry - what causes stability or instability - properties of various acids/bases and stability series - types of acids and bases - interpretation of pKa and pKaH values 2. Organic Chemistry - reaction mechanisms - carbonyl group chemistry (involving keto-enol chemistry, acetals, ketals, hemiacetals, hemiketals, organolithiums / Grignard reagents) - overview of functional groups - stereochemistry
Application of carbonyl group chemistry in organic synthesis: The material covered in this section includes (i) a-hydrogen acidity, (ii) acid and base promoted keto-enol tautomerism, (iii) a-enolate chemistry, including alkylation (iv) named reactions including Michael reaction, Aldol addition, Aldol condensation, Claisen condensation (v) ring-forming reactions including Dieckman condensation and Robinson annulations
- Class notes
- • 24 pages •
Application of carbonyl group chemistry in organic synthesis: The material covered in this section includes (i) a-hydrogen acidity, (ii) acid and base promoted keto-enol tautomerism, (iii) a-enolate chemistry, including alkylation (iv) named reactions including Michael reaction, Aldol addition, Aldol condensation, Claisen condensation (v) ring-forming reactions including Dieckman condensation and Robinson annulations
Pericyclic reactions. The material covered in this section includes (i) analysis of electrocyclic reactions, (ii) cycloaddition reactions and (iii) sigmatropic rearrangements by both a frontier orbital approach and by application of Woodward-Hoffmann rules.
- Class notes
- • 14 pages •
Pericyclic reactions. The material covered in this section includes (i) analysis of electrocyclic reactions, (ii) cycloaddition reactions and (iii) sigmatropic rearrangements by both a frontier orbital approach and by application of Woodward-Hoffmann rules.
Simplified notes on organic chemistry, providing an in depth , complete & well written description.
- Study guide
- • 8 pages •
Simplified notes on organic chemistry, providing an in depth , complete & well written description.
Includes 2017 CH306C (now CH326) exam paper and answers to all of section A and all parts if section B except the peptide chemistry questions
- Exam (elaborations)
- • 10 pages •
Includes 2017 CH306C (now CH326) exam paper and answers to all of section A and all parts if section B except the peptide chemistry questions
Includes 2018 CH306C (now CH326) exam paper and answers to all of section A and all parts if section B except the peptide chemistry questions
- Exam (elaborations)
- • 9 pages •
Includes 2018 CH306C (now CH326) exam paper and answers to all of section A and all parts if section B except the peptide chemistry questions
Includes 2019 CH326 exam paper and answers to all of section A and all parts of section B except peptide chemistry questions
- Exam (elaborations)
- • 9 pages •
Includes 2019 CH326 exam paper and answers to all of section A and all parts of section B except peptide chemistry questions
Includes 2019 January paper and answers
- Exam (elaborations)
- • 9 pages •
Includes 2019 January paper and answers
Includes answers for ALL questions in exam paper
- Exam (elaborations)
- • 10 pages •
Includes answers for ALL questions in exam paper
In this module you will be taking a mechanistic approach to introductory organic chemistry and learning about the major types of reactivity at carbon centres. The module will build on previous modules such as ‘Language of Chemistry’ and incorporate kinetics and spectroscopy, where appropriate, to build your understanding of reactivity at both carbon sp3 and sp2 centres. By the end of the module you will be able to predict and rationalise the outcomes of reactions at sp3 and sp2 centres, incl...
- Summary
- • 87 pages •
In this module you will be taking a mechanistic approach to introductory organic chemistry and learning about the major types of reactivity at carbon centres. The module will build on previous modules such as ‘Language of Chemistry’ and incorporate kinetics and spectroscopy, where appropriate, to build your understanding of reactivity at both carbon sp3 and sp2 centres. By the end of the module you will be able to predict and rationalise the outcomes of reactions at sp3 and sp2 centres, incl...
