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CH3-underset(CH3)underset(|)(CH)-CH3+ove...

`CH_3-underset(CH_3)underset(|)(CH)-CH_3+overset(Br_2)underset(hv)rarr(A)` . (Major) . A will be

A

`CH_3-underset(CH_3)underset(|)(CH)-CH_2Br`

B

`CH_3-underset(CH_3)underset(|)(CH)=CH_2`

C

`CH_3-underset(CH_3)underset(|)overset(Br)overset(|)(CH)-CH_3`

D

`CH_3-overset(CH_2)overset(|)(CH)=H_2Br`

Text Solution

AI Generated Solution

The correct Answer is:
To determine the major product (A) when the compound \( CH_3-CH(CH_3)-CH_3 \) reacts with bromine (\( Br_2 \)) in the presence of sunlight (hv), we will follow these steps: ### Step 1: Identify the Structure The compound \( CH_3-CH(CH_3)-CH_3 \) is 2-methylpropane (also known as isobutane). It has a branched structure with a central carbon atom connected to two methyl groups and one ethyl group. ### Step 2: Understand the Reaction Conditions The reaction involves bromination in the presence of sunlight. Sunlight provides energy that initiates the free radical halogenation mechanism. In this process, the \( Br-Br \) bond will break homolytically to form two bromine radicals. ### Step 3: Formation of Bromine Radicals When \( Br_2 \) is exposed to sunlight, it dissociates into two bromine radicals: \[ Br_2 \xrightarrow{hv} 2Br^{\cdot} \] ### Step 4: Free Radical Mechanism The bromine radicals can abstract hydrogen atoms from the alkane (2-methylpropane) to form free radicals. The abstraction can occur at different positions: - Primary hydrogen (from the terminal carbon) - Secondary hydrogen (from the central carbon) ### Step 5: Stability of Free Radicals The stability of the resulting free radicals is crucial in determining the major product. The stability order is: - Tertiary (3°) > Secondary (2°) > Primary (1°) In this case: - If a bromine radical abstracts a hydrogen from a primary carbon, a primary radical is formed. - If a bromine radical abstracts a hydrogen from the central carbon (which is secondary), a secondary radical is formed. Since secondary radicals are more stable than primary radicals, the major product will be formed from the secondary radical. ### Step 6: Product Formation The secondary radical will react with another bromine radical to form the major product: - The major product will be 2-bromo-2-methylpropane. ### Conclusion Thus, the major product \( A \) formed from the reaction of \( CH_3-CH(CH_3)-CH_3 \) with \( Br_2 \) in the presence of sunlight is: \[ A = 2-bromo-2-methylpropane \]
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