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Which of the following acids on heating ...

Which of the following acids on heating loses a molecul of `H_(2)O` to form an `alpha,beta`-unsaturated acid?

A

`CH_(3)CHOHCOOH`

B

`HOCH_(2)COOH`

C

`CH_(3)CHOHCH_(2)COOH`

D

`HOCH_(2)CH_(2)CH_(2)COOH`

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The correct Answer is:
To determine which of the given acids loses a molecule of water upon heating to form an alpha, beta-unsaturated acid, we need to analyze each option systematically. Here’s the step-by-step solution: ### Step 1: Understand the Structure of Alpha, Beta-Unsaturated Acids Alpha, beta-unsaturated acids are characterized by a double bond between the alpha and beta carbon atoms adjacent to the carboxylic acid group. The general structure can be represented as: - R-CH=CH-COOH Where R can be a hydrogen or any alkyl group. ### Step 2: Analyze Each Acid Option Let’s denote the acids as follows for clarity: 1. Acid A: R1-CHOH-COOH 2. Acid B: R2-CH2OH-COOH 3. Acid C: R3-CH(OH)-CH2-COOH 4. Acid D: R4-CH2-CH2-COOH We will analyze each option to see if heating leads to the loss of water (H2O) and the formation of an alpha, beta-unsaturated acid. ### Step 3: Evaluate Acid A For Acid A (R1-CHOH-COOH): - Upon heating, the hydroxyl group (OH) from the alpha carbon can combine with a hydrogen atom from the beta carbon to form water (H2O). - This results in the formation of R1-CH=COOH, which is an alpha, beta-unsaturated acid. ### Step 4: Evaluate Acid B For Acid B (R2-CH2OH-COOH): - Similar to Acid A, upon heating, the OH group can lose a hydrogen atom from the adjacent carbon, resulting in the formation of R2-CH=COOH, which is also an alpha, beta-unsaturated acid. ### Step 5: Evaluate Acid C For Acid C (R3-CH(OH)-CH2-COOH): - Upon heating, the OH group can again lose a hydrogen atom from the adjacent carbon, leading to the formation of R3-CH=CH-COOH, which is an alpha, beta-unsaturated acid. ### Step 6: Evaluate Acid D For Acid D (R4-CH2-CH2-COOH): - In this case, there is no hydroxyl group on the alpha or beta carbon. Thus, it cannot lose water to form an alpha, beta-unsaturated acid. ### Conclusion From the analysis, Acids A, B, and C can lose a molecule of water upon heating to form alpha, beta-unsaturated acids. However, Acid D does not have the necessary structure to undergo this reaction. ### Final Answer The correct options that can form alpha, beta-unsaturated acids upon heating are: - Acid A, Acid B, and Acid C.

To determine which of the given acids loses a molecule of water upon heating to form an alpha, beta-unsaturated acid, we need to analyze each option systematically. Here’s the step-by-step solution: ### Step 1: Understand the Structure of Alpha, Beta-Unsaturated Acids Alpha, beta-unsaturated acids are characterized by a double bond between the alpha and beta carbon atoms adjacent to the carboxylic acid group. The general structure can be represented as: - R-CH=CH-COOH Where R can be a hydrogen or any alkyl group. ### Step 2: Analyze Each Acid Option ...
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PRADEEP-ALDEHYDES, KETONES AND CARBOXYLIC ACIDS -COMPETITION FOCUS JEE (MAIN AND ADVANCED)/MEDICAL ENTRANCE SPECIEAL (MULTIPLE CHOICE QUESTIONS-I WITH ONE CORRECT ANSWER)
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