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The following compound is obtained by th...

The following compound is obtained by the reduction of benzoic acid with lithium alumimium hydride –

A

Cyclohexanoic acid

B

Benzylalcohol

C

Cyclohexa–1, 4–dioic acid

D

No reaction

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AI Generated Solution

The correct Answer is:
To solve the question regarding the compound obtained by the reduction of benzoic acid with lithium aluminium hydride (LiAlH4), we will follow these steps: ### Step 1: Identify the Reactants The reactant in this case is benzoic acid, which has the molecular formula C6H5COOH. It contains a carboxylic acid functional group (-COOH). **Hint:** Remember that benzoic acid is an aromatic carboxylic acid with a phenyl group attached to a carboxyl group. ### Step 2: Understand the Reducing Agent Lithium aluminium hydride (LiAlH4) is a strong reducing agent commonly used to reduce carboxylic acids to primary alcohols. **Hint:** LiAlH4 donates hydride ions (H-) which can reduce carbonyl groups. ### Step 3: Mechanism of Reduction 1. The hydride ion from LiAlH4 attacks the carbonyl carbon of the carboxylic acid, resulting in the formation of a tetrahedral intermediate. The carbonyl oxygen becomes negatively charged (alkoxide ion). 2. The tetrahedral intermediate can be represented as: - C6H5C(OH)(O-)H **Hint:** The attack of the hydride ion leads to the formation of a negatively charged oxygen. ### Step 4: Protonation of the Alkoxide In the presence of water (which is often used to quench the reaction), the negatively charged oxygen will pick up a proton (H+) from water, leading to the formation of a primary alcohol. 3. The product formed after protonation is benzyl alcohol (C6H5CH2OH). **Hint:** The final product is a primary alcohol, which is characterized by the -OH group attached to a carbon that is bonded to only one other carbon atom. ### Step 5: Conclusion The compound obtained from the reduction of benzoic acid with lithium aluminium hydride is benzyl alcohol. **Final Answer:** Benzyl alcohol (C6H5CH2OH). ### Summary of Options - Option 1: Cyclohexanoic acid - Incorrect - Option 2: Benzyl alcohol - Correct - Option 3: Cyclohexane-1,4-dioic acid - Incorrect - Option 4: No reaction - Incorrect **Correct Answer:** Option 2 - Benzyl alcohol.
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MOTION-CARBOXYLIC ACID-Exercise - 4 (LEVEL - 2 )
  1. The following compound is obtained by the reduction of benzoic acid wi...

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  2. The IUPAC name of C(6)H(5)COCl is

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  3. Which of the following reactants on reaction with conc. NaOH followed ...

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  4. Match the compounds in Column I with their characteristic test(s)/reac...

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  5. Match each of the compounds given in Column I with the reaction(s), th...

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  6. The major product of the following reaction is

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  7. Among the following compounds, the most acidic is

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  8. The carboxyl functional group (-COOH) is present in :

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  9. The compound that undergoes decarboxylation most readily under mild c...

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  10. After completion of the reaction (I and II), the organic compound(s) i...

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  11. P and Q are isomers of dicarboxylic acid C(4)H(4)O(4). Bothdecolorize ...

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  12. P and Q are isomer of dicraboxylic acid C(4)H(4)O(4) Both decolourixe ...

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  13. In the reaction shown, below, the major product(s) formed is/are :

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  14. Consider all possible isomeric ketones, including stereoisomers, of MW...

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  15. The product(s) of the following reaction sequence is(are):

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  16. Compound p and R upon ozonolysis produce Q and S, respectively . Th...

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  17. Columns 1,2 and 3 contain starting materials, reaction conditions, and...

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  18. Columns 1,2 and 3 contain starting materials, reaction conditions, and...

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  19. Columns 1,2 and 3 contain starting materials, reaction conditions, and...

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  20. Aniline reacts with mixed acid (cone. HNO(3) and cone. H(2)SO(4)) at 2...

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  21. Treatment of benzene with CO/HCl in the presence of anhydrous "AlCl"(3...

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