Claisen Study guides, Class notes & Summaries
Looking for the best study guides, study notes and summaries about Claisen? On this page you'll find 36 study documents about Claisen.
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![Organic Chemistry: Alpha-Beta Carbon Chemistry](/docpics/6317fa704d1b2_1944617.jpg)
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Organic Chemistry: Alpha-Beta Carbon Chemistry
- Class notes • 12 pages • 2022
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This chapter contains all necessary information needed to know about the alpha carbon chemistry of carbonyl compounds. These notes are color coded. It contains information about acidity, enolization, alpha halogenation, aldol and claisen condensation reactions, malonic and acetoacetic ester synthesis, conjugate addition and michael addition reactions. Reactions and mechanisms are shown clearly with arrows, and explanations as necessary.
![Test Bank for Lehninger Principles of Biochemistry 7th Edition by Nelson (complete, questions/answers/rationales)](/docpics/3063784/64b10ed33d0fa_3063784_121_171.jpeg)
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Test Bank for Lehninger Principles of Biochemistry 7th Edition by Nelson (complete, questions/answers/rationales)
- Exam (elaborations) • 9 pages • 2023
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1. If the delta G'° of the reaction A --> B is -40 kJ/mol, under standard conditions the reaction: 
 
A) is at equilibrium. 
B) will never reach equilibrium. 
C) will not occur spontaneously. 
D) will proceed at a rapid rate. 
E) will proceed spontaneously from A to B. 
E 
 
 
 
For the reaction A --->B, delta G'° = -60 kJ/mol. The reaction is started with 10 mmol of A; no B is initially present. After 24 hours, analysis reveals the presence of 2 mmol of B, 8 mmol of A. Which is the mo...
![organic chemistry 2 exam 4 material](/docpics/4064052/658351caefd74_4064052_121_171.jpeg)
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organic chemistry 2 exam 4 material
- Class notes • 11 pages • 2023
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covering all notes from exam 3 to exam 4. Clasen condensation, crossed claisen, Dieckman condensation, a-halogenation, aldol, LDA, NAH, acetoacetic ester, decarboxylation, malonic ester, conjugate addition, Michael reactions, azide/Gabriel synthesis, reductive animation, amines, Robinson annulation.
![Organic chemistry _General Organic Chemistry name reactions.](/docpics/3139973/64c24f64539fe_3139973_121_171.jpeg)
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Organic chemistry _General Organic Chemistry name reactions.
- Presentation • 12 pages • 2023
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Organic Chemistry name reactions with examples Mechanism & additional information in columns while looking at it you can differentiate between given name reactions very fast.You'll grasp faster just by looking at it. 
It include name reaction such as- 
 condensation 
2.Claisen reaction 
en Schmidt reaction 
e condensation 
in condensation 
ann condensation 
n reaction 
ngeal reaction 
ch reaction 
ro reaction 
orm reaction 
matsky reaction 
el addition reaction 
son ring annulation reaction. 
I...
![Discussion Notes on Enol Enolates and Enaminaes](/docpics/5585879/6664e41f18a3c_5585879_121_171.jpeg)
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Discussion Notes on Enol Enolates and Enaminaes
- Class notes • 10 pages • 2024
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Enol Enolates and Enamines: 
 
Enol Enolates: These are formed by deprotonating an alpha carbon adjacent to a carbonyl group in a molecule containing both a carbonyl and an enolizable proton. They are important intermediates in many organic reactions, particularly in aldol condensation and Claisen condensation reactions. 
 
Enamines: These are formed by the reaction of a secondary amine with a carbonyl compound, resulting in the formation of a carbon-nitrogen double bond. Enamines are versatile ...
![DAT Organic Chemistry Reactions](/docpics/2825121/6475c388d00f5_2825121_121_171.jpeg)
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DAT Organic Chemistry Reactions
- Exam (elaborations) • 13 pages • 2023
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--NO2 + Sn/HCl - Correct Answers>Clemmenson Reduction 
--NH2 
1,2-addition 
conj double bonds + RMgX or LiAlH4 - Correct Answers>Nucleophiles attack the carbonyl directly. Strong nucleophiles: Gringards, NaBH4, LiAlH4 
1. (2) esters CH3--C=O--OEt + NaOR, EtOH 
2. H3O+ 
 
ketone + (ester) CH3--C=O--OEt + -OR + H3O+ --> - Correct Answers>Claisen Condensation 
enolate ion of one ester acts as nucleophile attacking another ester 
 
1. NaOR, EtOH 2. H3O+ 
 
Anhydride for mixed 
1. BH3/TH...
![Class notes science](/docpics/3079091/64b56fdb887d3_3079091_121_171.jpeg)
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Class notes science
- Interview • 4 pages • 2023
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These lecture notes cover a wide range of topics, from the basics of molecular structure and bonding to the intricate mechanisms of organic reactions. Whether you're a beginner seeking a solid foundation or an advanced learner looking to deepen your knowledge, this resource caters to all levels of expertise
![Part 7 Organic Chemistry II Transesterification to Phenol Bromination](/docpics/63f1196b7c518_2385536.jpg)
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Part 7 Organic Chemistry II Transesterification to Phenol Bromination
- Summary • 20 pages • 2023
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All notes are taken from the textbook and summarized for easy learning. Pictures, diagrams, and synthesis reactions are made in great detail. These are the notes I used to get a 98 in the class.
Organic Chemistry: Structure and Function by Neil E. Shore and K. Peter C. Vollhardt. Chapter 22 review. Topics include benzyllic reactions and mechanisms.
![CHEM 309 Organic Chemistry II homework 10 With Completed Solutions- Boise State University](/docpics/644149a37f91a_2629270.jpg)
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CHEM 309 Organic Chemistry II homework 10 With Completed Solutions- Boise State University
- Exam (elaborations) • 4 pages • 2023
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CHEM 309 Organic Chemistry II homework 10 With Completed Solutions- Boise State University Acid chlorides are the most reactive carboxylic acid derivatives. Provide curved arrows to complete t he following reaction mechanism for attack of a typical neutral nucleophile to an acid chloride. Remember the rules for drawing curved arrows: begin each arrow at a bond or lone pair (draw them in) and end each arrow at an atom or bond. lb) When neutral nucleophiles react with acid chlorides or anhydrides-...
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