In the reaction with $H C l$ , an alkene reacts in accordance with the Markovnikov's rule, to give a product 1-chloro-1-methylcyclohexane. The possible alkene is:

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Solution

The correct option is C

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Q. In the reaction with

H C l

, an alkene reacts in accordance with the Markovnikov's rule, to give a product 1-chloro-1-methylcyclohexane. The possible alkene is:

Q. An alkene "A" on reaction with

O_{3}

and

Z n - H_{2} O

gives propanone and ethanal in equimolar ratio.
Addition of

H C l

to alkene

A

gives

B

as the major product. The structure of product

B

is:

Predict all the alkenes that would be formed by dehydrohalogenation of the following halides with sodium ethoxide in ethanol and identify the major alkene:

(i) 1-Bromo-1-methylcyclohexane

(ii) 2-Chloro-2-methylbutane

(iii) 2,2,3-Trimethyl-3-bromopentane.

A compound 'X' reacts with conc. Sulphuric acid to give an alkene. The alkene reacts with bromine and subsequent treatment of the product with alcoholic KOH yields propyne. The formula of the compound is

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In the reaction with HCl, an alkene reacts in accordance with the Markovnikov's rule, to give a product 1-chloro-1-methylcyclohexane. The possible alkene is:

The correct option is C

In the reaction with $H C l$ , an alkene reacts in accordance with the Markovnikov's rule, to give a product 1-chloro-1-methylcyclohexane. The possible alkene is: