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CH(3) CH (CH(3))CH(2)NH(2) overset( NaN...

`CH_(3) CH (CH_(3))CH_(2)NH_(2) overset( NaNO_(2)//HCI ) to (A) overset( aq.KOH ) to (B) ` compound (B ) is :

A

`CH_(3)CH(CH_(3))CH_2 OH`

B

`(CH_3)_2C(OH) C_2 H_5`

C

`(CH_3)_3COH`

D

None of these

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The correct Answer is:
To solve the question step by step, we will analyze the reactions involving the given amine and identify the products formed at each stage. ### Step 1: Identify the Given Amine The starting compound is **CH₃CH(CH₃)CH₂NH₂**, which is a primary amine. The structure can be represented as follows: - **CH₃** (methyl group) - **CH(CH₃)** (isopropyl group) - **CH₂** (methylene group) - **NH₂** (amino group) ### Step 2: Reaction with NaNO₂/HCl When the primary amine reacts with sodium nitrite (NaNO₂) in the presence of hydrochloric acid (HCl), it forms a diazonium salt. The reaction can be summarized as follows: - **CH₃CH(CH₃)CH₂NH₂ + NaNO₂/HCl → CH₃CH(CH₃)CH₂N₂⁺Cl⁻ (A)** The diazonium cation formed is **CH₃CH(CH₃)CH₂N₂⁺**. This compound is unstable and can decompose to form a carbocation. ### Step 3: Formation of Carbocation The diazonium salt can lose nitrogen gas (N₂) to form a carbocation: - **CH₃CH(CH₃)CH₂N₂⁺ → CH₃CH(CH₃)CH₂⁺ + N₂** Here, the carbocation formed is **CH₃CH(CH₃)CH₂⁺**, which is a secondary carbocation. ### Step 4: Reaction with Aqueous KOH The carbocation is then treated with aqueous KOH. The hydroxide ion (OH⁻) acts as a nucleophile and attacks the carbocation, leading to the formation of an alcohol: - **CH₃CH(CH₃)CH₂⁺ + OH⁻ → CH₃CH(CH₃)CH₂OH (B)** The product formed, **(B)**, is **CH₃CH(CH₃)CH₂OH**, which is 2-propanol (also known as isopropyl alcohol). ### Final Answer Thus, the compound (B) is **2-propanol (isopropyl alcohol)**. ---
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