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For the following bond cleavages, use curved-arrows to show the electron flow and classify as homolysis or heterolysis. Identify reactive intermediate produced as free radical, carbocation and - Chemistry

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प्रश्न

For the following bond cleavages, use curved-arrows to show the electron flow and classify as homolysis or heterolysis. Identify reactive intermediate produced as free radical, carbocation and carbanion.

टीपा लिहा

उत्तर

The bond cleavage using curved-arrows to show the electron flow of the given reaction can be represented as

It is an example of heterolytic cleavage as the bond breaks in such a manner that the shared pair of electrons remains with the bromine ion. The reaction intermediate formed is a carbocation.

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Fundamental Concepts in Organic Reaction Mechanism - Fission of a Covalent Bond
  या प्रश्नात किंवा उत्तरात काही त्रुटी आहे का?
पाठ 12: Organic Chemistry - Some Basic Principles and Techniques - EXERCISES [पृष्ठ ३७०]

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एनसीईआरटी Chemistry - Part 1 and 2 [English] Class 11
पाठ 12 Organic Chemistry - Some Basic Principles and Techniques
EXERCISES | Q 12.16 - (c) | पृष्ठ ३७०

संबंधित प्रश्‍न

For the following bond cleavages, use curved arrows to show the electron flow and classify homolysis or heterolysis. Identify reactive intermediate produced as free radical, carbocation and carbanion.

\[\ce{CH3O - OCH3 -> CH3\overset\bullet{\text{O}} + \overset\bullet{\text{O}}CH3}\]


For the following bond cleavages, use curved-arrows to show the electron flow and classify as homolysis or heterolysis. Identify reactive intermediate produced as free radical, carbocation and carbanion.


For the following bond cleavages, use curved-arrows to show the electron flow and classify as homolysis or heterolysis. Identify reactive intermediate produced as free radical, carbocation and carbanion.


Which of the following carbocation is most stable?


What is the correct order of decreasing stability of the following cations.

I. \[\ce{CH3 - \overset{⊕}{C}H - CH3}\]
II. \[\ce{CH3 - \overset{⊕}{C}H - OCH3}\]
III. \[\ce{CH3 - \overset{⊕}{C}H - CH2 - OCH3}\]

Covalent bond can undergo fission in two different ways. The correct representation involving a heterolytic fission of CH3 – Br is:


Write structures of various carbocations that can be obtained from 2-methylbutane. Arrange these carbocations in order of increasing stability.


Match the intermediates given in Column I with their probable structure in Column II.

Column I Column II
(i) Free radical (a) Trigonal planar
(ii) Carbocation (b) Pyramidal
(iii) Carbanion (c) Linear

Which of the following carbocation's is most stable?


(I) (II) (III) (IV)

Among the given species the resonance stabilised carbocations are:


Which of the following is the most stable carbocation?


A solution of (–) – 1 – chloro–1–phenylethane in toluene racemises slowly in the presence of a small amount of SbCl5, due to the formation of ______.


The increasing order of stability of the following free radicals is ______.


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