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C(6)H(5)CHO overset(NH(2)OH)(rarr)" A " ...

`C_(6)H_(5)CHO overset(NH_(2)OH)(rarr)" A " overset(H_(2)O)(rarr)` B
What is not true for the compound B –

A

Gives cannizaro’s reaction

B

Acts as strong reducing agent

C

Gives phenol on reduction

D

Gives optical active compound with HCN

Text Solution

AI Generated Solution

The correct Answer is:
To solve the problem, we need to analyze the reactions of the compound C₆H₅CHO (benzaldehyde) and determine the properties of the resulting compound B after the reactions. Let's break it down step by step. ### Step 1: Identify the Initial Compound The initial compound is C₆H₅CHO, which is benzaldehyde. It is a carbonyl compound and does not have any alpha-hydrogens. ### Step 2: Reaction with Hydroxylamine (NH₂OH) When benzaldehyde reacts with hydroxylamine (NH₂OH), a nucleophilic addition reaction occurs. The nitrogen from hydroxylamine attacks the carbonyl carbon, leading to the formation of an oxime. **Reaction:** C₆H₅CHO + NH₂OH → C₆H₅CH=NOH (Oxime) This product is referred to as compound A. ### Step 3: Hydrolysis of Compound A Next, we perform hydrolysis on the oxime (compound A) using water (H₂O). Hydrolysis will convert the oxime back to the original aldehyde. **Reaction:** C₆H₅CH=NOH + H₂O → C₆H₅CHO Thus, compound B is again benzaldehyde (C₆H₅CHO). ### Step 4: Analyze Properties of Compound B Now we need to evaluate the statements regarding compound B (benzaldehyde) and identify which statement is not true. 1. **Gibbs-Canizzaro Reaction:** - Benzaldehyde does not have alpha-hydrogens, so it can undergo the Canizzaro reaction. This statement is true. 2. **Acts as a Strong Reducing Agent:** - In the Canizzaro reaction, one molecule of benzaldehyde is oxidized while another is reduced. Therefore, it can act as a reducing agent. This statement is true. 3. **Gives Phenol on Reduction:** - When benzaldehyde is reduced, it forms benzyl alcohol (C₆H₅CH₂OH), not phenol (C₆H₅OH). This statement is not true. 4. **Gives Optical Active Compound with HCN:** - When benzaldehyde reacts with HCN, it forms a cyanohydrin, which has a chiral carbon and can be optically active. This statement is true. ### Conclusion The statement that is not true regarding compound B (benzaldehyde) is that it gives phenol on reduction. ### Final Answer The statement that is not true for compound B is: "Gives phenol on reduction." ---
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MOTION-CARBONL COMPOUNDS-EXERCISE -1
  1. A ketone reacted with ethyl magnesium bromide followed by hydrolysis g...

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  2. The reaction , 2RCHO overset("Al-ethoxide")(rarr) RCOOCH(2)R is called...

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  3. Aldol condensation between following compounds, followed by dehydratio...

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  4. In Cannizzaro reaction-

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  5. HCHO with conc. alkali forms two compounds. The change in oxidation nu...

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  6. Which is most difficult to oxidise-

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  7. C(6)H(5) "COCl" underset(H(2))overset(Pd-BaSO(4))(rarr) Intermediate ...

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  8. C(6)H(5)CHO overset(NH(2)OH)(rarr)" A " overset(H(2)O)(rarr) B What ...

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  9. Benzaldehyde can be converted to benzyl alcohol by –

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  10. Benzaldehyde condenses with acetic anhydride to give cinnamic acid in ...

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  11. ? underset(ETOH(2)H(2)O)overset(Delta, CN^(-))(rarr) Benzoin. The rea...

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  12. C(6)H(5)CHO overset(Cl(2))(rarr) A + HCl The product A when reacts ...

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  13. Acetone shows similarity with acetaldehyde in reacting to-

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  14. Which statement is true about benzaldehyde

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  15. Which of the following combinations give t-butyl alcohol when treated ...

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  16. The conversion CH(3)CH(2)CHO "––––"rarr CH(3)CH(2)CH(2)OH can not be a...

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  17. Which of the following can be used to differentiate between ethanal an...

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  18. Fehling’s solution –B is-

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  19. Acetone gives test with-

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  20. Which of the following does not turn Schiff's reagent to pink?

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