**Reaction Instructions**:Draw the **major product(s)** of the following reactions, if there is a reaction. **Be sure to include stereochemistry in your products.**1. **Reaction 1:** - Starting Material: Methyl acetate (\(CH_3COOCH_3\)) - Reagent: Sodium chloride (NaCl) - Outcome: No reaction. Methyl acetate does not react with sodium chloride under normal conditions.2. **Reaction 2:** - Starting Material: Ethyl acetate (\(CH_3COOCH_2CH_3\)) - Reagents: 1. Lithium aluminum hydride (LiAlH₄) 2. Acidic work-up (\(H_3O^+\)) - Outcome: Reduction of ester to the corresponding alcohol. The product will be ethanol (\(CH_3CH_2OH\)).3. **Reaction 3:** - Starting Material: Benzamide (\(C_6H_5CONH_2\)) - Reagents: 1. Lithium aluminum hydride (LiAlH₄) 2. Acidic work-up (\(H_3O^+\)) - Outcome: Reduction of amide to the corresponding amine. The product will be benzylamine (\(C_6H_5CH_2NH_2\)).

Answered: Draw the major product(s) of the…

Draw the major product(s) of the following reactions, if there is a reaction. Be sure to include stereochemistry in your products. Naci H3C OCH3 1. LIAIH4 2. Н,о* OCH3 1. LIAIH4 NH2 2. H30*

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Concept explainers

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.

Question

**Reaction Instructions**:

Draw the **major product(s)** of the following reactions, if there is a reaction. **Be sure to include stereochemistry in your products.**

1. **Reaction 1:**
- Starting Material: Methyl acetate (\(CH_3COOCH_3\))
- Reagent: Sodium chloride (NaCl)
- Outcome: No reaction. Methyl acetate does not react with sodium chloride under normal conditions.

2. **Reaction 2:**
- Starting Material: Ethyl acetate (\(CH_3COOCH_2CH_3\))
- Reagents:
1. Lithium aluminum hydride (LiAlH₄)
2. Acidic work-up (\(H_3O^+\))
- Outcome: Reduction of ester to the corresponding alcohol. The product will be ethanol (\(CH_3CH_2OH\)).

3. **Reaction 3:**
- Starting Material: Benzamide (\(C_6H_5CONH_2\))
- Reagents:
1. Lithium aluminum hydride (LiAlH₄)
2. Acidic work-up (\(H_3O^+\))
- Outcome: Reduction of amide to the corresponding amine. The product will be benzylamine (\(C_6H_5CH_2NH_2\)).

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