Questions

Which is more acidic COOH COOH or COOH CH2 COOH?

Which is more acidic COOH COOH or COOH CH2 COOH?

The carboxylic acid is acidic as it has hydrogen in the −COOH group. As we know, oxalic acid easily releases its H atom to form CH3COO− ion whereas formic acid needs more energy. Hence, the Strength of oxalic acid is more than formic acid. So, Oxalic acid (COOH-COOH) is more acidic than formic acid (HCOOH).

Which is more acidic CH3COOH or ch3clcooh?

Solution 1 Cl-CH2COOH is a stronger acid than CH3COOH : Chlorine is a electron withdrawing group and its increase the acidity of carboxylic acids by stabilising the conjugate base due to delocalisation of the negative charge by resonance effects.

Which of the following is more acidic CH2 COOH?

Cl-CH2-COOH(Chloroacetic acid) is more acidic than CH3-COOH(Acetic acid) because Chlorine(Cl) is a good electron withdrawing atom which produces a strong -I effect than that produced on acetic acid by CH3 group.

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Is FCH2COOH stronger than ClCH2COOH?

Since fluorine is most electronegative and strongest electron withdrawing group, therefore, fluoroacetic acid F CH2COOH is stronger as compared to chloro, bromo and iodo acetic acids.

Which of the following carboxylic acid is most acidic CH3 COOH CH3 CH2 COOH H COOH?

Correct option c HCOOHExplanation:Due to +I effect methyl group —COOH group has lesser acidic property so formic acid is more acidic in comparision to other given acids.

Which is more acidic and why CH2 CH COOH or CH3COOH?

– In propanoic acid (CH3-CH2-COOH), H atom is held strongly in -COOH due to resonance. – Due to presence of double bond in propenoic acid (CH2=CH-COOH), tendency of -COOH group to donate H atom is drastically increased. This makes it easier to deprotonate which increases acidity.

Which is more acidic ch3ch2cooh or CH3COOH?

ch3cooh is more acidic.

Which of the following is the strongest acid COOH?

So, the strongest acid is CCl$_3$COOH.

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Which is more acidic CH3COOH or FCH2COOH?

This is because the -I effect of the electronegative substituents results in the delocalization of the negative charge on the carboxyl carbon, making the release of H+ easier, and thus enhancing the acid strength. Thus, the least acidic is CH3COOH (acetic acid), and the most acidic is F2CHCOOH (difluoro acetic acid).

Which is more acidic Hcooh or FCH2COOH?

sequence in increasing acidic character: FCH2 COOH, CH3COOH, HCOOH. Thus as the distance between the electronegative group and the COOH group increases, the dispersal of the negative charge of the corresponding carboxylate ion becomes less pronounced and hence the acidic strength decreases.