o N 1. LiAlH 2. H₂O 4 NH 2

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Nitriles are reduced to primary amines when reacting with lithium aluminum hydride (LiAlH4) followed by H2O. Using curved arrows, draw the mechanism for nitrile reduction with LiAlH4 for the reaction shown. Be sure to include lone pairs and charges where relevant.
The image displays a chemical reaction involving a pyridine molecule and a hydride donor:

- On the left, there is a cyclic compound with a five-membered ring containing one nitrogen atom. This structure represents pyridine with a nitrile group (C≡N) attached.

- In the middle, there is a hydride reagent formula shown as H-AlH₃¯, indicating the presence of an aluminum hydride complex.

- An arrow on the right suggests progression to the next step in the reaction or formation of an end product.

This reaction likely involves the reduction of the nitrile group by the aluminum hydride reagent.
Transcribed Image Text:The image displays a chemical reaction involving a pyridine molecule and a hydride donor: - On the left, there is a cyclic compound with a five-membered ring containing one nitrogen atom. This structure represents pyridine with a nitrile group (C≡N) attached. - In the middle, there is a hydride reagent formula shown as H-AlH₃¯, indicating the presence of an aluminum hydride complex. - An arrow on the right suggests progression to the next step in the reaction or formation of an end product. This reaction likely involves the reduction of the nitrile group by the aluminum hydride reagent.
This image illustrates a chemical reaction converting a nitrile to an amine. The reaction begins with a five-membered cyclic compound containing a nitrile group (C≡N) attached to the ring. 

The reaction proceeds in two steps:

1. **LiAlH₄**: Lithium aluminum hydride is used as a reducing agent. It reduces the nitrile group to an amine group.

2. **H₂O**: Water is added to complete the reaction, resulting in the final product, an amine.

The product is a five-membered cyclic compound with an -NH₂ group, indicating the conversion of the nitrile to an amine. This transformation is commonly used in organic chemistry to synthesize amines from nitriles.
Transcribed Image Text:This image illustrates a chemical reaction converting a nitrile to an amine. The reaction begins with a five-membered cyclic compound containing a nitrile group (C≡N) attached to the ring. The reaction proceeds in two steps: 1. **LiAlH₄**: Lithium aluminum hydride is used as a reducing agent. It reduces the nitrile group to an amine group. 2. **H₂O**: Water is added to complete the reaction, resulting in the final product, an amine. The product is a five-membered cyclic compound with an -NH₂ group, indicating the conversion of the nitrile to an amine. This transformation is commonly used in organic chemistry to synthesize amines from nitriles.
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