Enolate Study guides, Class notes & Summaries

Enolates of derivatives, Decarboxylation, Fatty Acid introduction notes

--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...

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.

What are (2) other names for the TCA cycle? 1) Tricarboxylic acid cycle 2) Krebs Cycle When acetyl-CoA enters the TCA cycle, what molecule is it condensed with? Oxaloacetate How many CO₂ molecules are released during the TCA cycle? 2 What are molecules are generated by the TCA cycle from a single acetyl-CoA (pyruvate) molecule? 3 NADH 1 QH₂ 1 XTP (X = G or A) How much energy (i.e., ATP) is gained from the TCA cycle if a single molecule of acetyl-CoA feeds i...

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-...

Chapter section review 7.7-7.9. Covers tautomerization, acidity of alpha protons, and tautomerization mechanisms and explanation.

Different Nitrogen names - ANSWER Enamine: C=C-N Amine : C-N Imine: C=N Amide: O=C-N Imide: O=C-N-C=O Ketone(aldehyde) + 1° amine --> Imine Ketone(aldehyde) + 2° amine ---> Enamine think about it when replace the Oxygen of carbonyl and attach NitrogenR, /Make sure It has a lone pair. for the 2 ° amine move double bond to the C. Amine - ANSWER C-N Myopia (nearsighted) - ANSWER *(-)F= diverging mirror /convex mirror/concave lens *convex mirror: image always virtual...

List of all the common reactions learned in Organic Chemistry 2.

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...

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...