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Action of hydrogen chloride on CH3-under...

Action of hydrogen chloride on `CH_3-underset(CH_3)underset|C=CH_2` and on `CH-=CH` will predominantly give the compounds, reapectively

A

`CH_3-undersetunderset(CH_3)(|)CH-CH_2Cl` and `CH_2Cl-CH_2Cl`

B

`CH_3-undersetunderset(CH_3)|"CCl"-CH_3` and `CH_3-CHCl_2`

C

`CH_3-undersetunderset(CH_3)(|)CH-CH_2Cl` and `CH_3-CHCl_2`

D

`CH_3-undersetunderset(CH_3)|CH-CH_3` and `CH_2Cl-CH_2Cl`

Text Solution

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The correct Answer is:
To solve the problem of the action of hydrogen chloride (HCl) on the compounds `CH3C(CH3)=CH2` (isobutene) and `CH≡CH` (acetylene), we can follow these steps: ### Step 1: Identify the Compounds The first compound is isobutene, which has the structure `CH3C(CH3)=CH2`. The second compound is acetylene, which has the structure `CH≡CH`. ### Step 2: Reaction of HCl with Isobutene When HCl is added to isobutene, an electrophilic addition reaction occurs. The double bond in isobutene acts as a nucleophile and attacks the hydrogen (H+) from HCl. 1. The H+ from HCl adds to one of the carbon atoms in the double bond, forming a carbocation. The more stable carbocation is formed by adding H+ to the carbon that is more substituted (the one attached to two methyl groups). 2. The resulting carbocation is `CH3C+(CH3)CH2`, which is a tertiary carbocation. 3. The Cl- ion from HCl then attacks the carbocation, resulting in the product `CH3C(CH3)ClCH2`. ### Step 3: Reaction of HCl with Acetylene When HCl is added to acetylene, a similar electrophilic addition reaction occurs, but since acetylene has a triple bond, the reaction will happen twice. 1. The first addition of HCl to acetylene results in the formation of a vinyl carbocation: `CH2=C^+(H)CH`. 2. The Cl- ion then attacks this carbocation, forming `CH2Cl-CH=CH2` (vinyl chloride). 3. A second addition of HCl will occur, leading to the formation of a geminal dihalide: `CHCl2-CH2`. ### Final Products - The product from the reaction of HCl with isobutene is `CH3C(CH3)ClCH2` (2-chloro-2-methylpropane). - The product from the reaction of HCl with acetylene is `CHCl2-CH2` (1,1-dichloroethane). ### Summary of Products 1. For isobutene (`CH3C(CH3)=CH2`), the predominant product is `CH3C(CH3)ClCH2`. 2. For acetylene (`CH≡CH`), the predominant product is `CHCl2-CH2`.

To solve the problem of the action of hydrogen chloride (HCl) on the compounds `CH3C(CH3)=CH2` (isobutene) and `CH≡CH` (acetylene), we can follow these steps: ### Step 1: Identify the Compounds The first compound is isobutene, which has the structure `CH3C(CH3)=CH2`. The second compound is acetylene, which has the structure `CH≡CH`. ### Step 2: Reaction of HCl with Isobutene When HCl is added to isobutene, an electrophilic addition reaction occurs. The double bond in isobutene acts as a nucleophile and attacks the hydrogen (H+) from HCl. ...
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