Answered step by step
Verified Expert Solution
Link Copied!

Question

1 Approved Answer

Question 6. Imagine you want to deprotonate cyclohexanone in the most efficient way possible (i.e. with the highest conversion to products). Of the bases given,

image text in transcribed

Question 6. Imagine you want to deprotonate cyclohexanone in the most efficient way possible (i.e. with the highest conversion to products). Of the bases given, which one(s) would you choose? Why? (1 page, 4 marks) "Base" H-Base cyclohexanone pka 24.8 Bases to choose from (pka's given are of their corresponding conjugated acids, i.e. H-Base): KOH triethylamine (pka = 10.8) lithium diisopropylamine (LDA, pka - 36) 4-dimethylaminopyridine (DMAP, pka 9.2) butyllithium (Buli, pka-60) potassium hydroxide pka 15.7

Step by Step Solution

There are 3 Steps involved in it

Step: 1

blur-text-image

Get Instant Access to Expert-Tailored Solutions

See step-by-step solutions with expert insights and AI powered tools for academic success

Step: 2

blur-text-image

Step: 3

blur-text-image

Ace Your Homework with AI

Get the answers you need in no time with our AI-driven, step-by-step assistance

Get Started

Recommended Textbook for

Elementary Principles of Chemical Processes

Authors: Richard M. Felder, ‎ Ronald W. Rousseau, ‎ Lisa G. Bullard

4th edition

978-1118431221, 9781119192138, 1118431227, 1119192137, 978-1119498759

More Books

Students also viewed these Chemical Engineering questions