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Benzoic acid is stronger than methanoic ...

Benzoic acid is stronger than methanoic acid but weaker than ethanoic acid. True or False

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To determine whether the statement "Benzoic acid is stronger than methanoic acid but weaker than ethanoic acid" is true or false, we need to analyze the acidity of the three acids involved: benzoic acid, methanoic acid, and ethanoic acid. ### Step-by-Step Solution: 1. **Identify the Structures of the Acids**: - **Methanoic Acid (HCOOH)**: This is the simplest carboxylic acid with no alkyl groups attached to the carboxyl group. - **Ethanoic Acid (CH3COOH)**: This acid has a methyl group (CH3) attached to the carboxyl group. - **Benzoic Acid (C6H5COOH)**: This acid has a carboxyl group attached to a benzene ring. 2. **Understanding Acidity**: - The strength of an acid is often determined by its ability to donate a proton (H+). The stability of the resulting conjugate base also plays a crucial role in acidity. - The presence of alkyl groups can influence acidity through inductive effects. Alkyl groups generally have a +I (electron-donating) effect, which can destabilize the negative charge on the conjugate base, making the acid weaker. 3. **Comparing Methanoic Acid and Ethanoic Acid**: - Methanoic acid (HCOOH) does not have any alkyl groups, so it does not experience the destabilizing +I effect. - Ethanoic acid (CH3COOH) has a methyl group, which exerts a +I effect, increasing electron density on the carboxylate ion (the conjugate base), making it a weaker acid compared to methanoic acid. - **Conclusion**: Methanoic acid is stronger than ethanoic acid. 4. **Comparing Benzoic Acid and Ethanoic Acid**: - Benzoic acid has a carboxyl group attached to an sp2 hybridized carbon in the benzene ring. The resonance stabilization provided by the benzene ring can help stabilize the negative charge on the benzoate ion (the conjugate base). - Ethanoic acid, with its sp3 hybridized carbon, is less stable due to the +I effect of the methyl group. - **Conclusion**: Benzoic acid is stronger than ethanoic acid. 5. **Final Evaluation of the Statement**: - The statement claims that benzoic acid is stronger than methanoic acid but weaker than ethanoic acid. - From our analysis, we found that: - Methanoic acid > Ethanoic acid - Benzoic acid > Ethanoic acid - Therefore, the statement is **False** because benzoic acid is not weaker than methanoic acid. ### Final Answer: **False**
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Ortho effect is special type of effect that is shown by o-subsituents .This ortho-effect operates at the benzoic acids irrespective of the polar type. Nearly all o-substituted benzoic acid are stronger than benzoic acid. Benzoic acid is a resonance stabilised and so the carboxyl group is coplaner with the ring. An o-subsituent tends to prevent this coplanarity. Which among the following will be the strongest acid ?

Ortho effect is special type of effect that is shown by o-subsituents .This ortho-effect operates at the benzoic acids irrespective of the polar type. Nearly all o-substituted benzoic acid are stronger than benzoic acid. Benzoic acid is a resonance stabilised and so the carboxyl group is coplaner with the ring. An o-subsituent tends to prevent this coplanarity. What is the order of K_(a) of following compounds ?

Explain why formic acid is stronger acid than benzoic acid.

Assertion : Benzoic acid is stronger acid than acetic acid. Reason : K_(a) for benzoic acid is 6.5xx10^(-5) and for acetic acid is 1.74xx10^(-5) .

ALLEN-ALKENE, ALKANE & ALKYNE -EXCERSISE-3
  1. Heating of beta-hydroxy acid gives lactones.

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  2. Hunsdiecker reaction involve free radical in intermediate steps.

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  3. Benzoic acid is stronger than methanoic acid but weaker than ethanoic ...

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  4. Acid halides are more reactive than acid amides towards the hydrolysis...

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  5. What happens when sodium benzoate is heated with soda lime?

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  6. pK(a) and K(a) of an acid are connected by the relation.......

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  7. Fill in the blank by choosing the appropriate word/words from those gi...

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  8. Hell-Volhard-Zelinsky reaction involves the replacement of an ...........

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  9. Carboxylic acids may be prepared by the reaction of Grigrand reagents ...

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  10. Statement-I: Unlike the gtC=O group of aldehydes and ketones, the C=O ...

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  11. Statement-I: CH(3)COCH(2)COOC(2)H(5) will give iodoform test. Becau...

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  12. Statement-1: Acetic acid does not undergo haloform test. and State...

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  13. Statement-I: Benzoic acid on nitration will give m- nitro benzoic ac...

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  14. Statement-I: Acyl halide are more reactive than acid substance amide t...

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  15. Amides undergo hydrolysis to yield carboxylic acid plus amine on heati...

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  16. Amides undergo hydrolysis to yield carboxylic acid plus amine on heati...

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  17. Acid halides are more reactive than acid amides towards the hydrolysis...

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  18. When is treated with two equivalent of methyl magnesium iodide a...

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  19. Ester gives nucleophilic addition reaction followed by elimination rea...

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  20. Ester gives nucleophilic addition reaction followed by elimination rea...

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