Suppose the following reaction:
Benzene $(C_6H_6) + CH_3-CH=CH_2$ $\xrightarrow{H^{\oplus}} A$ $\xrightarrow{O_2} B$ $\xrightarrow{H^{\oplus} / \Delta} C + CH_3-CO-CH_3$
The structure of intermediate compound $B$ will be

  • A
    Phenol
  • B
    Isopropyl phenyl ether
  • C
    Cumene hydroperoxide
  • D
    $2-$phenyl$-1-$propanol hydroperoxide

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Which among the following has the highest melting point?

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Given below are two statements:
Statement $I$: The acidic strength of monosubstituted nitrophenol is higher than phenol because of the electron-withdrawing nitro group.
Statement $II$: $o$-nitrophenol,$m$-nitrophenol,and $p$-nitrophenol will have the same acidic strength as they have one nitro group attached to the phenolic ring.
In the light of the above statements,choose the most appropriate answer from the options given below:

What is formed on heating an aqueous solution of benzene diazonium chloride?

What happens when $phenol$ reacts with bromine water?

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