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Reaction of benzamide, KOH and bromine y...

Reaction of benzamide, KOH and bromine yields :

A

Benzene

B

Bromobezene

C

Aniline

D

Acetanilide

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To solve the question regarding the reaction of benzamide with KOH and bromine, we can follow these steps: ### Step-by-Step Solution: 1. **Identify the Reactants**: The reactants are benzamide (C6H5CONH2), KOH (potassium hydroxide), and bromine (Br2). 2. **Deprotonation of Benzamide**: The KOH acts as a strong base and deprotonates the amide nitrogen in benzamide. This results in the formation of a negatively charged amide ion (C6H5C(O)NH). \[ \text{C}_6\text{H}_5\text{C(O)NH}_2 + \text{KOH} \rightarrow \text{C}_6\text{H}_5\text{C(O)N}^- + \text{H}_2\text{O} \] 3. **Formation of N-Bromoamide**: The negatively charged amide ion can now react with bromine. The bromine molecule (Br2) will react with the amide ion, resulting in the substitution of a bromine atom for the hydrogen atom on the nitrogen. This forms N-bromoamide. \[ \text{C}_6\text{H}_5\text{C(O)N}^- + \text{Br}_2 \rightarrow \text{C}_6\text{H}_5\text{C(O)NBr} + \text{Br}^- \] 4. **Formation of an Imine**: The N-bromoamide can undergo further reaction with KOH. The hydroxide ion (OH^-) can abstract a proton from the nitrogen, generating a double bond between carbon and nitrogen, resulting in the formation of an imine. \[ \text{C}_6\text{H}_5\text{C(O)NBr} + \text{KOH} \rightarrow \text{C}_6\text{H}_5\text{C=NBr} + \text{H}_2\text{O} \] 5. **Hydrolysis of the Imine**: The imine can be hydrolyzed in the presence of water (from KOH) to yield benzamide again, but with the release of carbon dioxide (CO2) and the formation of a primary amine. \[ \text{C}_6\text{H}_5\text{C=NBr} + \text{H}_2\text{O} \rightarrow \text{C}_6\text{H}_5\text{C(O)NH}_2 + \text{CO}_2 + \text{Br}^- \] 6. **Final Product**: The final product of the reaction is benzamide (C6H5C(O)NH2) along with the release of carbon dioxide and bromide ion. ### Conclusion: The reaction of benzamide with KOH and bromine yields benzamide again, along with the release of CO2 and Br^-. ---

To solve the question regarding the reaction of benzamide with KOH and bromine, we can follow these steps: ### Step-by-Step Solution: 1. **Identify the Reactants**: The reactants are benzamide (C6H5CONH2), KOH (potassium hydroxide), and bromine (Br2). 2. **Deprotonation of Benzamide**: The KOH acts as a strong base and deprotonates the amide nitrogen in benzamide. This results in the formation of a negatively charged amide ion (C6H5C(O)NH). ...
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NARAYNA-ALDEHYDES, KETONES & CARBOXYLIC ACIDS-EXERCISE -II (H.W.)
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  2. An or ganic acid was converted into its calcium salt and it was dry di...

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  3. A sequential reaction may be performed as represented below : "RCH"...

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  4. Reaction of benzamide, KOH and bromine yields :

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  5. Which of the following has the maximum acidic strength?

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  6. Action of benzoic acid with hydroazoic acid in presence of conc. H(2)S...

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  7. Sulphonation of benzoic acid produces mainly

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  8. The general formula of both aldehyde & ketone is

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  9. When acetylene is passed through dil.H(2)SO(4) in the presence of HgSO...

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  10. Aldehydes are first oxidation product of :

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  11. Formalin is the commercial name of :

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  12. The compound that will not give indoform on treatment with alkali and ...

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  13. Tollen's reagent is :

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  14. Urotropine is formed by the action of ammonia on:

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  15. When acetaldehyde is treated with ammoniacal silver nitrate solution ,...

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  16. The reverse of esterification process is called:

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  17. 2CH(3) "CHO" overset(Al(OC(2)H(5))(3))(rarr) CH(3) "COOCH"(2)CH(3) ...

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  18. Explain the reactivity of acyl compounds in the order:

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  19. Acetic anhydride on readuction with LiAlH"(4) in ether gives :

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  20. In presence of red phosphorus catalyst, chlorine reacts with acetic ac...

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