Enolate Study guides, Class notes & Summaries
Looking for the best study guides, study notes and summaries about Enolate? On this page you'll find 41 study documents about Enolate.
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Organic Chemistry 2: Summary of Alpha Carbon Chemistry
- Summary • 10 pages • 2022
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This document is a summary of the alpha carbon chemistry chapter of the organic chemistry 2 course. It is digitally taken handwritten notes. 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, enolizations, alpha halogenations, aldol and claisen condensation reactions, malonic and acetoacetic ester synthesis, conjugate addition and michael addition reactions. Rea...
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Course Title: Solomons 11e Chapter Number: 18
- Exam (elaborations) • 40 pages • 2022
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Package Title: Solomons Test Bank Course Title: Solomons 11e Chapter Number: 18 Question type: Multiple Choice 1) Which of the compounds listed below is more acidic than 1-butanol? a) Ethyl acetoacetate b) 2-Butanone c) Ethyl pentanoate d) All of these choices. e) Two of these choices. Answer: A Topic: Relative Acidities Section: 18.1 Difficulty Level: Medium 2) Which of the compounds listed below is more acidic than 1-butanol? a) Diethylmalonate b) 2-Butanone c) Ethyl pentanoate d) All of these...
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Organic Chemistry Notes: Enolate ions, Enols, and alpha-beta unsaturated carbonyl compounds
- Class notes • 3 pages • 2021
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In depth notes including plenty of diagrams and chemical reactions.
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Answer key for Mid-term 2 exam Form A(1)
- Exam (elaborations) • 12 pages • 2021
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CHEM 2420 ---Organic Chemistry II 
Fall 2015 
Mid-Exam No. 2: Chapter 17-18 (Form A) 
Name: ÿ'ÿ,ÿt ÿ-,4 
Instructions: 
A) Please print your name on the line above. 
B) Make sure you have 12 pages. 
C) Good luck! 
Question Score 
Multiple choice /80 
Free response 
Bonus 
Total 
/20 
/5 
/105 
1 IP aÿ.,o e 
Section 1. Multiple Choice (80 points) 
Bubble the choice that best completes each phrase and/or answers the question on the Scantron sheet 
provided. Answers written in this section of...
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CHEM008C ( Enol, Alkylations, Acylation)
- Class notes • 9 pages • 2020
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Learn about enols, halogenation, alkylation, and acylation in depth with written arrow pushing mechanisms and written definitions.
And that's how you make extra money
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Final Exam Study Guide (Enols and Enolates, Amines, Polymers)
- Study guide • 7 pages • 2019
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Reactions and details covered from Dr. Feducia's Orgo 2 lecture from Summer 19.
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Exam 2 Study Guide (Suzuki Chemistry, Aldehydes and Ketones, Carboxylic Acids and Derivatives, Enols and Enolates)
- Study guide • 11 pages • 2019
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Reactions and details covered from Dr. Feducia's Orgo 2 class in Summer 19.
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Monofunctional Carbonyls Notes
- Class notes • 18 pages • 2020
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Carbanions are looked at with examples and how to stabilise through inductive and resonance effects. Enolate formation reaction is introduced and a look at different bases and how complete deprotonation can be. The stabilisation of enolates develops the topic before the α-halogenation by base or acid catalysed reactions. More enolate reactions are given. Alkylate aldehydes formation through enamines. Aldol reaction through acid and base conditions in either equilibrating and non-equilibrating c...
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Carbonyl Group Chemistry
- Class notes • 24 pages • 2020
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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
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Advance organic chemistry
- Manual • 280 pages • 2019
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This manual is a good book for students of chemistry, pharmacists and chemical engineering. It has 8 topics such as isomers, nucleophilic addition, enolate reactions, mechanisms of reaction, reduction and oxidation, molecular bonding of carbon and hybridization, etc.
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