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Is methyl an electron withdrawing group?

Dortha Miller ∙

Lvl 10

∙ 9mo ago

Updated: 2/7/2025

Yes, methyl is not an electron withdrawing group.

AnswerBot

∙ 9mo ago

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Is the methyl group in a molecule electron donating or withdrawing?

The methyl group in a molecule is electron donating.

Is ch3 an electron withdrawing group?

Yes, CH3 (methyl group) is considered an electron donating group rather than an electron withdrawing group.

Is methyl electron donating or withdrawing?

Methyl is electron donating.

Is OCH3 an electron-withdrawing group?

Yes, OCH3 is an electron-withdrawing group.

Is nitrogen an electron withdrawing group?

Yes, nitrogen is an electron withdrawing group.

Related Questions

Is the methyl group in a molecule electron donating or withdrawing?

The methyl group in a molecule is electron donating.

Is ch3 an electron withdrawing group?

Yes, CH3 (methyl group) is considered an electron donating group rather than an electron withdrawing group.

Is methyl electron donating or withdrawing?

Methyl is electron donating.

Is OCH3 an electron-withdrawing group?

Yes, OCH3 is an electron-withdrawing group.

Is nitrogen an electron withdrawing group?

Yes, nitrogen is an electron withdrawing group.

Is the BR group electron donating or withdrawing?

The BR group is electron withdrawing.

Is the carbonyl group electron withdrawing or donating?

The carbonyl group is electron withdrawing.

Is ome an electron withdrawing group?

Yes, the carbonyl group (CO) is an electron-withdrawing group.

Is BR considered an electron withdrawing group?

Yes, BR is considered an electron withdrawing group.

Is a ketone considered an electron withdrawing group?

Yes, a ketone is considered an electron withdrawing group.

Is methoxy considered an electron withdrawing group?

Yes, methoxy is considered an electron withdrawing group.

Which is more acidic butanoic acid or 3 methyl butanoic acid?

3-methyl butanoic acid is more acidic than butanoic acid because the presence of the methyl group in 3-methyl butanoic acid increases the electron-withdrawing effect, making the molecule more acidic by stabilizing the conjugate base.

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