Log out Go to App
Go to App

Learning Materials

Features

Discover

Chapter 12: PROBLEM 12.20 (page 475)

Question: What alkene yields each set of oxidative cleavage products?

a.

b.

Short Answer

Expert verified

Answer

a.

b.

c.

Step by step solution

01

Oxidative cleavage

In oxidative cleavage, the double bond is broken, and two carbonyl groups are formed.

Therefore, to yield a set of alkenes, the two carbonyls carbon should be joined together by eliminating the oxygen

02

Set of alkenes of oxidative cleavage

a.

Alkenes set

b.

Alkenes set

c.

Alkenes set

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.

Start your free trial

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

Question: Identify compounds A, B, and C.

a. Compound A has molecular formula C8H12 and reacts with two equivalents of H2. A gives HCOCH2CH2CHOas the only product of oxidative cleavage with O3followed byCH3SCH3.

b. Compound B has molecular formula C6H10and gives (CH3)2CHCH2CH2CH3 when treated with excess H2 in the presence of Pd. B reacts with NaNH2and CH3Ito form compound C (molecular formula C7H12).

Question:Devise a synthesis of (3R,4S)-3,4-dichlorohexane from acetylene and any needed organic compounds or inorganic reagents.

Question:What epoxide is formed when each alkene is treated with mCPBA?

a.

b.


c.

Question: Devise a synthesis of each compound from CH3CH2OHas the only organic starting material; that is, every carbon in the product must come from a molecule of ethanol. You may use any other needed inorganic reagents.

Draw the organic products formed when cyclopentene is treated with each reagent. With some reagents, no reaction occurs.

a. H2+Pd-C

b. H2+ Lindlar catalyst

c. Na ,NH3

d. CH3CO3H

e. [1]. CH3CO3H [2] H2O ,OH-

f. [1] OSO4+NMO [2] NaHSO3, H2O

g.KMnO4 ,H2O ,OH-

h. [1] LiAlH4 [2] H2O

i. [1] O3 .[2] H3CSCH3

j. (CH3)3COOH ,Ti [OCH(CH3)3]4 (-) DET

k. mCPBA

l.Product in (k); Then[1] LiAlH4 [2] H2O

See all solutions

Recommended explanations on Chemistry Textbooks

Nuclear Chemistry

Read Explanation

Kinetics

Read Explanation

Ionic and Molecular Compounds

Read Explanation

Chemical Analysis

Read Explanation

Making Measurements

Read Explanation

Organic Chemistry

Read Explanation
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