90873 Action of hydrogen iodide on anisole gives,

90878 An Assertion and a Reason are given below. Choose the correct answer from the following options.
Assertion (A) : Vinyl halides do not under go nucleophilic substitution easily.
Reason (R) : $\quad$ Even though the intermediate carbocation is stabilised by loosely held $\pi$-electrons, the cleavage is difficult because of strong bonding.

90879 $\mathbf{R}-\mathbf{X}+\mathbf{A} \rightarrow \mathbf{R N C}+\mathrm{B} ; \mathbf{A}$ and $\mathrm{B}$ are

90881 Neopentyl chloride reacts with benzene in presence of a Lewis acid $\left(\mathrm{AlCl}_{3}\right)$ to form

1

2

3

4

90873 Action of hydrogen iodide on anisole gives,

90878 An Assertion and a Reason are given below. Choose the correct answer from the following options.
Assertion (A) : Vinyl halides do not under go nucleophilic substitution easily.
Reason (R) : $\quad$ Even though the intermediate carbocation is stabilised by loosely held $\pi$-electrons, the cleavage is difficult because of strong bonding.

90879 $\mathbf{R}-\mathbf{X}+\mathbf{A} \rightarrow \mathbf{R N C}+\mathrm{B} ; \mathbf{A}$ and $\mathrm{B}$ are

90881 Neopentyl chloride reacts with benzene in presence of a Lewis acid $\left(\mathrm{AlCl}_{3}\right)$ to form

1

2

3

4

90873 Action of hydrogen iodide on anisole gives,

90878 An Assertion and a Reason are given below. Choose the correct answer from the following options.
Assertion (A) : Vinyl halides do not under go nucleophilic substitution easily.
Reason (R) : $\quad$ Even though the intermediate carbocation is stabilised by loosely held $\pi$-electrons, the cleavage is difficult because of strong bonding.

90879 $\mathbf{R}-\mathbf{X}+\mathbf{A} \rightarrow \mathbf{R N C}+\mathrm{B} ; \mathbf{A}$ and $\mathrm{B}$ are

90881 Neopentyl chloride reacts with benzene in presence of a Lewis acid $\left(\mathrm{AlCl}_{3}\right)$ to form

1

2

3

4

90873 Action of hydrogen iodide on anisole gives,

90878 An Assertion and a Reason are given below. Choose the correct answer from the following options.
Assertion (A) : Vinyl halides do not under go nucleophilic substitution easily.
Reason (R) : $\quad$ Even though the intermediate carbocation is stabilised by loosely held $\pi$-electrons, the cleavage is difficult because of strong bonding.

90879 $\mathbf{R}-\mathbf{X}+\mathbf{A} \rightarrow \mathbf{R N C}+\mathrm{B} ; \mathbf{A}$ and $\mathrm{B}$ are

90881 Neopentyl chloride reacts with benzene in presence of a Lewis acid $\left(\mathrm{AlCl}_{3}\right)$ to form

1

2

3

4