Which of the following will be most easily at | vedclass

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(B) Due to the strong $+M$ (mesomeric) effect of the $-OH$ group,the electron density on the benzene ring increases significantly,especially at the or

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Phenol

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(B) Due to the strong $+M$ (mesomeric) effect of the $-OH$ group,the electron density on the benzene ring increases significantly,especially at the ortho and para positions. This makes the ring highly activated towards electrophilic aromatic substitution. In contrast,$-Cl$ has a $-I$ effect that deactivates the ring,and $-CH_3$ has a weaker $+I$ and hyperconjugation effect compared to the $+M$ effect of $-OH$.

Which of the following will be most easily attacked by an electrophile?

Similar Questions

Assertion: Phenyl is used as a household germicide.
Reason: Phenyl is a phenol derivative and phenol is an effective germicide.

Which statement is true?

The major product of the given reaction is
$3-methoxyphenol$ $\xrightarrow[{(ii) \ H_2SO_4, \ heat}]{{(i) \ OHCCH_2COCl}}$

Identify the correct order of acidic strength for the following compounds:
$I$. Ortho-nitrophenol
$II$. Para-nitrophenol
$III$. Meta-nitrophenol

The correct options for the products $A$ and $B$ of the following reactions are:

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