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An isonitrile on reduction gives...

An isonitrile on reduction gives

A

`1^@` amine

B

`2^@` amine

C

`3^@` amine

D

quaternary ammonium salt

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To solve the question "An isonitrile on reduction gives," we will follow these steps: ### Step 1: Understand the Structure of Isonitrile Isonitriles, also known as isocyanides, have the functional group -N≡C. The general structure can be represented as R-N≡C, where R is an alkyl or aryl group. For example, methyl isonitrile would be CH3-N≡C. **Hint:** Recall the structure of isonitriles and their functional group. ### Step 2: Identify the Reduction Process Reduction typically involves the gain of hydrogen or the loss of oxygen. In the case of isonitriles, reduction will convert the isonitrile group (-N≡C) into an amine. The triple bond between nitrogen and carbon will be reduced to a single bond. **Hint:** Remember that reduction changes multiple bonds to single bonds by adding hydrogen. ### Step 3: Determine the Product of the Reduction When an isonitrile undergoes reduction, it will convert to an amine. The nitrogen in the isonitrile will form bonds with hydrogen and carbon. Specifically, the nitrogen will form three bonds: two with carbon atoms (from the original isonitrile and the new hydrogen added) and one with a hydrogen atom. For example, if we reduce methyl isonitrile (CH3-N≡C), the product will be a secondary amine, specifically dimethylamine (CH3-NH-CH3). **Hint:** Focus on how many carbon atoms are bonded to the nitrogen after reduction. ### Step 4: Classify the Type of Amine In the product formed, the nitrogen atom is bonded to two carbon atoms (from the original isonitrile and the new hydrogen added) and one hydrogen atom. This means that the resulting amine is a secondary amine, as it is attached to two carbon groups. **Hint:** Recall the classification of amines: primary (1 carbon), secondary (2 carbons), tertiary (3 carbons), and quaternary ammonium salts (4 substituents). ### Conclusion Thus, when an isonitrile is reduced, it gives a secondary amine. **Final Answer:** The correct answer is **b) secondary amine**.

To solve the question "An isonitrile on reduction gives," we will follow these steps: ### Step 1: Understand the Structure of Isonitrile Isonitriles, also known as isocyanides, have the functional group -N≡C. The general structure can be represented as R-N≡C, where R is an alkyl or aryl group. For example, methyl isonitrile would be CH3-N≡C. **Hint:** Recall the structure of isonitriles and their functional group. ### Step 2: Identify the Reduction Process ...
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ICSE-ORGANIC COMPOUNDS CONTAINING NITROGEN-EXERCISE (PART-I OBJECTIVE QUESTIONS)
  1. Phenyl isocyanides are prepared by

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  2. The compound obtained by reducing CH3 CN with Na//C2 H5 OH is

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  3. An isonitrile on reduction gives

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  4. Hydrolysis of benzonitrile gives

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  5. Conversion of nitrobenzene to aniline is carried out in

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  6. Towards electrophilic substitution, the most reactive will be

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  7. Acetanilide is prepared by the reaction of acetyl chloride on

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  8. Which of the following gives carbylamine reaction?

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  9. The compound obtained by heating a mixture of a primary amine and chlo...

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  10. which of the following reactions will not give a primary amine ?

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  11. Gabrial synthesis is used for the preparation of

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  12. Nitrosoamines (R2 N-N=O) are insoluble in water. On heating them with ...

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  13. Which of the following is a 3^@ amine?

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  14. The correct IUPAC name for CH2=CHCH2NHCH3 is

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  15. Amongst the following, the strongest base in aqueous medium is .

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  16. Which of the following is the weakest Bronsted base?

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  17. Benzyl amine may be alkylated as shown in the following equation : ...

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  18. Which of the following reagents would not be a good choice for reducin...

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  19. In order to prepare a 1^(@) amine from an alkyl halide with simultaneo...

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  20. The souce of nitrogen in Gabriel synthesis of amines is

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