Which of the following compounds would you expect to undergo aldol self-condensation? Show the product of each successful reaction.

(a) Trimethyl acetaldehyde

(b) Cyclobutanone

(c) Benzophenone (diphenyl ketone)

(d) 3-Pentanone

(e) Decanal

(f) 3-Phenyl-2-propenal

Short Answer

Expert verified

Aldol condensation occurs in those aldehydes and ketones which have acidic𝛂-hydrogen and on treatment with a base it gives𝛃-hydroxy aldehydes and ketones.

Step by step solution

01

(a)Trimethyl acetaldehyde 

Since it does not contain 𝛂-hydrogen therefore this compound does not give an aldol self-condensation reaction.

02

(b) Cyclobutanone

03

(c) Benzophenone (diphenyl ketone)      

Since the Benzophenone does not contain𝛂-hydrogen therefore this compound does not give an aldol self-condensation reaction.

04

(d) 3-Pentanone

05

(e) Decanal                                                          

06

(f) 3-Phenyl-2-propenal

3-Phenyl-2-propenal does not undergo aldol self-condensation since its𝛂-hydrogen is not acidic.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free