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Consider the following sequence of react...

Consider the following sequence of reaction and identify the final product (Z). `CH_3-CH=CH_2overset(HBr)rarr(X)overset(Aq.NaOH)rarr(Y)overset(NaOH+l_2)rarr(Z)`

A

`CH_3CHICH_3`

B

`CH_3CH_2CH_2I`

C

`CHI_3`

D

`CH_3COCH_3`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem step by step, we will analyze the sequence of reactions provided: 1. **Starting Material**: The starting compound is propene, which is represented as \( CH_3-CH=CH_2 \). 2. **First Reaction (with HBr)**: - Propene undergoes an electrophilic addition reaction with HBr. - Since propene is an unsymmetrical alkene, the addition follows Markovnikov's rule, where the bromine atom will attach to the more substituted carbon atom. - The reaction can be represented as follows: \[ CH_3-CH=CH_2 + HBr \rightarrow CH_3-CH(Br)-CH_3 \] - The product (X) is 2-bromopropane, \( CH_3-CH(Br)-CH_3 \). 3. **Second Reaction (with Aq. NaOH)**: - The product (X) is then treated with aqueous NaOH, which leads to a nucleophilic substitution reaction. - The hydroxide ion (\( OH^- \)) replaces the bromine atom: \[ CH_3-CH(Br)-CH_3 + NaOH \rightarrow CH_3-CH(OH)-CH_3 + NaBr \] - The product (Y) is 2-propanol (isopropanol), \( CH_3-CH(OH)-CH_3 \). 4. **Third Reaction (with NaOH + I2)**: - The final product (Y) is treated with NaOH and iodine (\( I_2 \)), which indicates that it will undergo the iodoform reaction. - The iodoform reaction occurs with compounds that have a methyl ketone group or secondary alcohols that can be oxidized to form methyl ketones. - In this case, 2-propanol can be oxidized to acetone, which is a methyl ketone: \[ CH_3-CH(OH)-CH_3 \xrightarrow{NaOH + I_2} CH_3-C(=O)-CH_3 \] - The acetone then reacts with iodine to form iodoform (\( CHI_3 \)): \[ CH_3-C(=O)-CH_3 \xrightarrow{I_2} CHI_3 + byproducts \] - The final product (Z) is iodoform, \( CHI_3 \). Thus, the final product (Z) is \( CHI_3 \). ### Summary of Steps: 1. Start with propene \( CH_3-CH=CH_2 \). 2. Add HBr to form 2-bromopropane \( CH_3-CH(Br)-CH_3 \). 3. Treat with aqueous NaOH to form 2-propanol \( CH_3-CH(OH)-CH_3 \). 4. React with NaOH and iodine to yield iodoform \( CHI_3 \).
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