/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Q.55C Question: Arrange the carbocatio... [FREE SOLUTION] | 91影视

91影视

Log out

Learning Materials

Features

Discover

Chapter 11: Q.55C (page 350)

Question: Arrange the carbocations below, in order of increasing stability.

c.

Short Answer

Expert verified

Answer

Step by step solution

01

Stability of carbocation

Rules for the stability of carbocation:

  1. More the resonance in the system more stable is the carbocation
  2. More the hyperconjugation that is the number of hydrogen with respect to the carbocation more stable is the carbocation
  3. More is the conjugation with a double bond in the molecule more stable is the carbocation
02

Order for Stability of carbocation

On the basis

Rule 2: More the hyperconjugation that is number of -hydrogen with respect to the carbocation more stable is the carbocation

Order of the stability of carbocation

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 91影视!

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

Compound X is optically inactive and has the formulaC16H16Br2. On treatment with strong base, X gives hydrocarbon Y,C16H14. Compound Y absorbs 2 equivalents of hydrogen when reduced over a palladium catalyst and reacts with ozone to give two fragments. One fragment, Z, is an aldehyde with formulaC7H6O. The other fragment is glyoxal,(CHO)2. Write the reactions involved, and suggest structures for X, Y, and Z. What is the stereochemistry of X?

Question: The reactions shown below are unlikely to occur as written. Tell what is wrong with each, and predict the actual product.

c.


Question:What products would you expect from the reaction of 1-bromopropane with each of the following?

(e) Na+-颁鈮贬

Question: Arrange the carbocations below, in order of increasing stability:

b.

What effect would you expect the following changes to have on the rate of the reaction of ethanol with 2-iodo-2-methyl butane?

(a) The concentration of the halide is tripled.
See all solutions

Recommended explanations on Chemistry Textbooks

Nuclear Chemistry

Read Explanation

Chemical Analysis

Read Explanation

The Earths Atmosphere

Read Explanation

Chemical Reactions

Read Explanation

Ionic and Molecular Compounds

Read Explanation

Inorganic 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.