Which of the following is not correct?

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(NONE) Let us analyze each option:$A$: The order of acidic strength for methylbenzoic acids is $o- > m- > p-$. This is correct due to the ortho effect

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(NONE) Let us analyze each option:$A$: The order of acidic strength for methylbenzoic acids is $o- > m- > p-$. This is correct due to the ortho effect and electronic effects.$B$: The stability of the carbocation with a positive charge adjacent to an oxygen atom is significantly higher due to resonance stabilization by the lone pair on oxygen. The given order is correct.$C$: The $-I$ effect of the chlorine atom increases the acidity of chloroacetic acid compared to formic acid. The order $ClCH_2-COOH > H-COOH$ is correct.$D$: The correct order of acidic strength for nitrophenols is $p-Nitrophenol > o-Nitrophenol > m-Nitrophenol$. This is correct due to the strong $-I$ and $-M$ effects of the nitro group at ortho and para positions,with para being stronger due to less steric hindrance and effective resonance.

Similar Questions

The correct order of stability for the following alkoxides is:
$(A)$ $CH_3CH(NO_2)O^-$
$(B)$ $CH_2=C(NO_2)O^-$
$(C)$ $O_2N-CH=CH-O^-$

Given below are two statements:
Statement $I:$ Hyperconjugation is a permanent effect.
Statement $II:$ Hyperconjugation in ethyl cation $(CH_{3}CH_{2}^{+})$ involves the overlapping of $C_{sp^{3}}-H_{1s}$ bond with the empty $2p$ orbital of the adjacent carbon.
Choose the correct option:

From the following,identify the groups that exhibit negative resonance $(-R)$ effect when attached to a conjugated system: $(A)$ formyl,$(B)$ amino,$(C)$ alkoxy,$(D)$ cyano,$(E)$ nitro

Identify the most acidic hydrogen present in the given compound.

Which among the following is an incorrect statement?

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