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Which of the following reagents would no...

Which of the following reagents would not be a good choice for reducing an aryl nitro compound to an amine?

A

`H_2`(excess)/Pt

B

`LiAlH_4` in ether

C

Fe and HCI

D

Sn and HCI

Text Solution

AI Generated Solution

The correct Answer is:
To determine which reagent would not be a good choice for reducing an aryl nitro compound to an amine, we can analyze each of the given reagents and their reactions with an aryl nitro compound. ### Step-by-Step Solution: 1. **Identify the Aryl Nitro Compound**: - An aryl nitro compound typically has a benzene ring with a nitro group (-NO2) attached. For example, we can consider nitrobenzene (C6H5NO2) as our starting compound. 2. **Evaluate the Reagents**: - We have four reagents to consider. Let's analyze each one individually. 3. **Reagent 1: H2 in the presence of Palladium (Pd)**: - This reagent is a common catalytic hydrogenation method. When nitrobenzene is treated with hydrogen in the presence of palladium, it reduces the nitro group to an amine group (-NH2), yielding aniline (C6H5NH2). - **Conclusion**: This is a good choice for reduction. 4. **Reagent 2: Lithium Aluminium Hydride (LiAlH4) in Dry Ether**: - LiAlH4 is a strong reducing agent. However, when it reacts with nitro compounds, it can lead to the formation of azo compounds rather than amines. In this case, it can produce azobenzene (C6H5-N=N-C6H5) instead of aniline. - **Conclusion**: This reagent is not a good choice for reducing an aryl nitro compound to an amine. 5. **Reagent 3: Iron (Fe) and Hydrochloric Acid (HCl)**: - Iron in the presence of HCl is another effective method for reducing nitro groups to amines. It will convert nitrobenzene to aniline. - **Conclusion**: This is a good choice for reduction. 6. **Reagent 4: Tin (Sn) and Hydrochloric Acid (HCl)**: - Similar to iron, tin with HCl can also reduce nitro groups to amines. It will also yield aniline from nitrobenzene. - **Conclusion**: This is a good choice for reduction. ### Final Answer: The reagent that would not be a good choice for reducing an aryl nitro compound to an amine is **Lithium Aluminium Hydride (LiAlH4) in dry ether**.

To determine which reagent would not be a good choice for reducing an aryl nitro compound to an amine, we can analyze each of the given reagents and their reactions with an aryl nitro compound. ### Step-by-Step Solution: 1. **Identify the Aryl Nitro Compound**: - An aryl nitro compound typically has a benzene ring with a nitro group (-NO2) attached. For example, we can consider nitrobenzene (C6H5NO2) as our starting compound. 2. **Evaluate the Reagents**: ...
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