Predict the product(s) of the following reaction. The given image depicts a chemical reaction sequence involving an epoxide. The structure shown is an epoxide ring with a wedge bond, indicating the three-dimensional arrangement of the molecule.**Steps in the Reaction Sequence:**1. **NH₃ (Ammonia)** - The first step involves the use of ammonia (NH₃) as a reagent. Ammonia can act as a nucleophile and attack the epoxide ring, leading to the ring-opening.2. **NaOH (Sodium Hydroxide)** - The second step uses sodium hydroxide (NaOH). This step might be used to deprotonate any resulting hydroxyl group after the ring opening, enhancing further reactivity.3. **Acid Chloride (CH₃COCl)** - In the third step, the acid chloride (CH₃COCl) is introduced. This step likely involves the acylation of the product from the previous step, resulting in the formation of an amide.The sequence indicates a transformation beginning with an epoxide, followed by nucleophilic attack and acylation to achieve an amide product. This reaction pathway is typical in organic synthesis for the functionalization of epoxides.

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Answered: 1. NH3 2. NaÕH 3. `CI

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1. NH3 2. NaÕH 3. `CI

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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Question

Predict the product(s) of the following reaction.

The given image depicts a chemical reaction sequence involving an epoxide. The structure shown is an epoxide ring with a wedge bond, indicating the three-dimensional arrangement of the molecule.

**Steps in the Reaction Sequence:**

1. **NH₃ (Ammonia)**
- The first step involves the use of ammonia (NH₃) as a reagent. Ammonia can act as a nucleophile and attack the epoxide ring, leading to the ring-opening.

2. **NaOH (Sodium Hydroxide)**
- The second step uses sodium hydroxide (NaOH). This step might be used to deprotonate any resulting hydroxyl group after the ring opening, enhancing further reactivity.

3. **Acid Chloride (CH₃COCl)**
- In the third step, the acid chloride (CH₃COCl) is introduced. This step likely involves the acylation of the product from the previous step, resulting in the formation of an amide.

The sequence indicates a transformation beginning with an epoxide, followed by nucleophilic attack and acylation to achieve an amide product. This reaction pathway is typical in organic synthesis for the functionalization of epoxides.

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