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A new C-C bond is formed in-...

A new C-C bond is formed in-

A

(a)Cannizzaro reaction

B

(b)Friedel Crafts reaction

C

(c)Both A `&` B

D

(d)None of these

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The correct Answer is:
To solve the question "A new C-C bond is formed in-", we need to analyze the given options: Kenny's arrow reaction, Friedel-Craft reaction, Both A and B, and None of these. ### Step-by-Step Solution: 1. **Understanding Kenny's Arrow Reaction**: - In Kenny's arrow reaction, an aldehyde reacts with a base (OH-). - The hydroxide ion (OH-) attacks the carbon of the aldehyde, forming an intermediate. - This intermediate can react with another aldehyde to produce carboxylic acid and primary alcohol. - **Conclusion**: In this process, no new carbon-carbon (C-C) bond is formed. 2. **Understanding Friedel-Crafts Reaction**: - In the Friedel-Crafts reaction, an alkyl halide (e.g., RCl) reacts with a Lewis acid (e.g., FeCl3). - This reaction generates a carbocation (R+) from the alkyl halide. - The carbocation then reacts with benzene, resulting in the formation of an alkyl-substituted benzene. - **Conclusion**: This process involves the formation of a new carbon-carbon (C-C) bond between the alkyl group and the benzene ring. 3. **Evaluating the Options**: - **Option A (Kenny's Arrow Reaction)**: No C-C bond is formed. - **Option B (Friedel-Crafts Reaction)**: A new C-C bond is formed. - **Option C (Both A and B)**: This is incorrect since Kenny's arrow does not form a C-C bond. - **Option D (None of these)**: This is also incorrect since Friedel-Crafts does form a C-C bond. 4. **Final Answer**: - The correct answer is **B (Friedel-Crafts reaction)**, as it is the only reaction among the options that results in the formation of a new carbon-carbon bond.
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ALLEN-ALKENE, ALKANE & ALKYNE -EXERCISE-5
  1. The most unlikely resonating structures of pnitrophenoxide ion is :

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  2. The reaction of with HBr gives :

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  3. A new C-C bond is formed in-

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  4. Benzenediazonium chloride on reaction with phenol in weakly basic medi...

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  5. Toluene, when treated with Br(2)Fe, gives o and p-bromotoluene, becaus...

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  6. Among the following, the strongest base is:

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  7. Identify the correct order of reactivity in electrophilic substitution...

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  8. (A) overset(NaNO(2)//HCl)underset((ii)H(2)//Ni)underset(0-5^(@))(rarr)...

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  9. Major product in this reaction is :

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  10. 4-Methyl benzene sulphoic acid reacts with sodium acetate to give :

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  11. +Cl-CH(2)CH(2)CH(3)overset(AlCl(3))(rarr) P underset((ii)H(2)O)overset...

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  12. RCONH2 is converted into RNH2 by means of Hofmann bromamide degradatio...

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  13. RCONH2 is converted into RNH2 by means of Hofmann bromamide degradatio...

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  14. RCONH2 is converted into RNH2 by means of Hofmann bromamide degradatio...

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  15. Gases released in reaction (I) and (II) are:

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  16. Order of boiling point for the following compounds is-

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  17. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

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  18. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

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  19. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

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  20. Reimer-Tiemann reaction introduces an aldehyde group on to the aromati...

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