Explain the reaction for the formation of acetal and hemiacetal.Explain why N,N-disubstituted amide is less acidic than ester.Why only methyl ketone do undergoes haloform reaction.LDA is the base of choice for carbonyl compound to completely convert into enolate. Why?

Since you have asked multiple question, we will solve the first question for you.If you want any…

Answered: Explain

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter25: Enolate & Enol Nucleophiles

Section: Chapter Questions

Problem 16E

See similar textbooks

Related questions

Question

Explain the reaction for the formation of acetal and hemiacetal.
Explain why N,N-disubstituted amide is less acidic than ester.
Why only methyl ketone do undergoes haloform reaction.
LDA is the base of choice for carbonyl compound to completely convert into enolate. Why?

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Expert Solution

Step by step

Solved in 2 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions