What is the product of the following reaction | vedclass

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(A) The reaction is an electrophilic aromatic substitution. $1$. The $H_2SO_4$ provides $H^+$ ions which protonate the alkene $Ph-C(CH_3)=CH_2$ to for

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(A) The reaction is an electrophilic aromatic substitution. $1$. The $H_2SO_4$ provides $H^+$ ions which protonate the alkene $Ph-C(CH_3)=CH_2$ to form a stable tertiary carbocation $Ph-C^+(CH_3)_2$. $2$. This carbocation acts as an electrophile and attacks the electron-rich benzene ring of anisole $(Ph-OCH_3)$. $3$. Since the $-OCH_3$ group is ortho/para directing,the bulky carbocation attacks the para-position due to steric hindrance at the ortho-position. $4$. The final product is $1-methoxy-4-(2-phenylpropan-2-yl)benzene$.

What is the product of the following reaction?

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Identify the correct order of reactivity of the following haloarenes on treatment with $NaOH$?

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The major product for the above reaction is:

Arrange the following set of compounds in order of their decreasing relative reactivity with an electrophile,$E^{+}$:
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