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Dipolar ion structure for amino acid is...

Dipolar ion structure for amino acid is

A

`H_(2)N-underset(R)underset(|)(CH)-COOH`

B

`H_(2)N-underset(R)underset(|)(CH)-COO^(+)`

C

`H_(3)^(+)N-underset(R)underset(|)(CH)-COO^(-)`

D

None of these

Text Solution

AI Generated Solution

The correct Answer is:
To determine the dipolar ion structure (zwitterion) for an amino acid, we need to understand the structure of amino acids and how they behave in solution. Here’s a step-by-step explanation: ### Step-by-Step Solution: 1. **Identify the Structure of an Amino Acid**: - An amino acid consists of a central carbon atom (C) bonded to an amino group (-NH2), a carboxyl group (-COOH), a hydrogen atom (H), and a variable R group (side chain). 2. **Understand the Concept of Zwitterion**: - A zwitterion is a molecule that has both positive and negative charges but is overall electrically neutral. In the case of amino acids, this occurs when the amino group is protonated (gains a hydrogen ion) and the carboxyl group is deprotonated (loses a hydrogen ion). 3. **Protonation and Deprotonation**: - In an aqueous solution, the amino group (-NH2) can accept a proton (H+) to become -NH3+ (positively charged). - The carboxyl group (-COOH) can lose a proton (H+) to become -COO- (negatively charged). 4. **Formation of the Zwitterion**: - When the amino acid is in solution, it exists predominantly as a zwitterion: - The amino group is positively charged (-NH3+). - The carboxyl group is negatively charged (-COO-). - The overall structure can be represented as: ``` R | H2N⁺ - C - COO⁻ | H ``` 5. **Charge Distribution**: - The positive charge on the amino group and the negative charge on the carboxyl group balance each other, making the molecule neutral overall, which is characteristic of zwitterions. 6. **Conclusion**: - The dipolar ion structure of an amino acid in solution is thus a zwitterion, where the amino group is positively charged and the carboxyl group is negatively charged.
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MOTION-CARBOXYLIC ACID-Exercise - 2(LEVEL - 2)
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  2. The bromination of aniline in presence of water produces :

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  3. The compound which on rection with aqueous nirous acid at low temperat...

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  4. Carbylamine test is performed in alcoholic KOH by heating a mixture of...

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  5. Activation of benzene by -NH2 group can be reduced by treating the com...

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  6. Dipolar ion structure for amino acid is

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  7. -NH(2) group shows acidic nature while reacts with reagent.

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  8. Which of the following does not give ethylamine on reduction

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  9. CH3 NH2 overset( "excess " CH3 Cl) to (X ) underset( "moist ") ...

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  10. The product not obtained in the following reaction , CH (3) - NO2...

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  11. Which of the following amines from N- nitroso derivative when treated ...

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  12. The strongest base among the following is

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  13. Identfiy compound (A) in the following oxidation reaction.

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  14. p-Cl-C(6)H(4)NH(2) and PhNH(3)^(+)Cl^(-) can be distinguished by

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  15. Acetamide is treated Separately with the following reagents. Which one...

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  16. Treatment of ammonia with excess of ethyl chloride will yield

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  17. C(6)H(5)C-=N and C(6)H(5)N-=C exhibit which type of isomerism

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  18. The correct reagent sequence for the following conversion CH(3)-unde...

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  19. Correct water solubility order/is amongst the following pairs is/are.

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  20. The correct order/s for the given pair of isomers is /are

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