### Predict the Expected Product and Provide IUPAC Names#### Instructions:You are given a sequence of reactions. Predict the expected product for each reaction and provide the IUPAC name for the correct reagent used to yield the desired epoxide.#### Reaction Sequence:1. **First Reaction:** - **Starting Material:** Cyclopentene (a five-membered ring with one double bond). - **Reagent:** [To be named - "NAME"] - ***Product:* An epoxide (a three-membered cyclic ether with the oxygen atom inserted across the double bond of cyclopentene).**2. **Second Reaction:** - **Starting Material:** The epoxide produced in the first reaction. - **Reagent:** HBr (Hydrogen Bromide) - **Product:** [To be identified - "2"]#### Multiple Choice for the Final Product:A. ![Cyclopentane with two bromine (Br) atoms on adjacent carbons](https://example.com/structure_A)B. ![Cyclopentane with a bromine (Br) and a hydroxyl (OH) group on adjacent carbons](https://example.com/structure_B)C. ![Cyclopentane with two hydroxyl (OH) groups on adjacent carbons](https://example.com/structure_C)D. ![Cyclopentane with an hydroxyl (OH) group and a bromine (Br) on adjacent carbons](https://example.com/structure_D)#### Graphical Explanations of Each Product:- **Option A:** Cyclopentane with two bromine (Br) atoms on adjacent carbons. - **Diagram:** A five-membered ring with two bromine atoms attached to adjacent carbons.- **Option B:** Cyclopentane with one bromine (Br) and one hydroxyl (OH) group on adjacent carbons. - **Diagram:** A five-membered ring with a bromine atom on one carbon adjacent to a carbon with a hydroxyl group.- **Option C:** Cyclopentane with two hydroxyl (OH) groups on adjacent carbons. - **Diagram:** A five-membered ring with hydroxyl groups attached to two adjacent carbons.- **Option D:** Cyclopentane with one hydroxyl (OH) group and one bromine (Br) group on adjacent carbons. - **Diagram **Predict the Expected Product for Each Reaction and Provide IUPAC Name for the Correct Starting Material to Yield the Desired Epoxide**---In this exercise, you are given a chemical reaction where a starting material reacts with mCPBA to form an epoxide, which then undergoes further reactions with NaSH followed by H2O to form a final product. Your task is to identify the expected final product from the provided options (A, B, C, D) and to provide the IUPAC name of the correct starting material in Box 1.### Reaction Overview:1. **First Step:** - The starting material (labeled as "NAME") reacts with mCPBA (meta-Chloroperoxybenzoic acid) to form an epoxide.2. **Second Step:** - The epoxide product then reacts with NaSH (sodium hydrosulfide) and H2O (water) to yield the final product.### Final Product Options:- **A:** Molecule with two thiol groups (-SH).- **B:** Molecule with one hydroxyl group (-OH) and one thiol group (-SH).- **C:** Molecule with two hydroxyl groups (-OH).- **D:** Molecule with one hydroxyl group (-OH) and one thiol group (-SH), but in different positions from option B.### Instructions:1. Based on the epoxidation and subsequent ring opening reactions, predict which compound (A, B, C, or D) will be the final product.2. Provide the IUPAC name of the correct starting material in Box 1.---**Box 1 (name):** [Your Answer Here]

Under acidic condition, epoxide opens from greater substituted side while under basic condition from…

Answered: Predict the expected product for each…

Predict the expected product for each reaction and provide IUPAC name for the correct reagent used to yield the desired epoxide: A Br Br NAME B OH Br HBr C OH OH ? D Br OH

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

Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.

Question

### Predict the Expected Product and Provide IUPAC Names

#### Instructions:
You are given a sequence of reactions. Predict the expected product for each reaction and provide the IUPAC name for the correct reagent used to yield the desired epoxide.

#### Reaction Sequence:

1. **First Reaction:**
- **Starting Material:** Cyclopentene (a five-membered ring with one double bond).
- **Reagent:** [To be named - "NAME"]
- ***Product:* An epoxide (a three-membered cyclic ether with the oxygen atom inserted across the double bond of cyclopentene).**

2. **Second Reaction:**
- **Starting Material:** The epoxide produced in the first reaction.
- **Reagent:** HBr (Hydrogen Bromide)
- **Product:** [To be identified - "2"]

#### Multiple Choice for the Final Product:

A. ![Cyclopentane with two bromine (Br) atoms on adjacent carbons](https://example.com/structure_A)

B. ![Cyclopentane with a bromine (Br) and a hydroxyl (OH) group on adjacent carbons](https://example.com/structure_B)

C. ![Cyclopentane with two hydroxyl (OH) groups on adjacent carbons](https://example.com/structure_C)

D. ![Cyclopentane with an hydroxyl (OH) group and a bromine (Br) on adjacent carbons](https://example.com/structure_D)

#### Graphical Explanations of Each Product:

- **Option A:** Cyclopentane with two bromine (Br) atoms on adjacent carbons.
- **Diagram:** A five-membered ring with two bromine atoms attached to adjacent carbons.

- **Option B:** Cyclopentane with one bromine (Br) and one hydroxyl (OH) group on adjacent carbons.
- **Diagram:** A five-membered ring with a bromine atom on one carbon adjacent to a carbon with a hydroxyl group.

- **Option C:** Cyclopentane with two hydroxyl (OH) groups on adjacent carbons.
- **Diagram:** A five-membered ring with hydroxyl groups attached to two adjacent carbons.

- **Option D:** Cyclopentane with one hydroxyl (OH) group and one bromine (Br) group on adjacent carbons.
- **Diagram

**Predict the Expected Product for Each Reaction and Provide IUPAC Name for the Correct Starting Material to Yield the Desired Epoxide**

---

In this exercise, you are given a chemical reaction where a starting material reacts with mCPBA to form an epoxide, which then undergoes further reactions with NaSH followed by H2O to form a final product. Your task is to identify the expected final product from the provided options (A, B, C, D) and to provide the IUPAC name of the correct starting material in Box 1.

### Reaction Overview:

1. **First Step:**
- The starting material (labeled as "NAME") reacts with mCPBA (meta-Chloroperoxybenzoic acid) to form an epoxide.

2. **Second Step:**
- The epoxide product then reacts with NaSH (sodium hydrosulfide) and H2O (water) to yield the final product.

### Final Product Options:

- **A:** Molecule with two thiol groups (-SH).
- **B:** Molecule with one hydroxyl group (-OH) and one thiol group (-SH).
- **C:** Molecule with two hydroxyl groups (-OH).
- **D:** Molecule with one hydroxyl group (-OH) and one thiol group (-SH), but in different positions from option B.

### Instructions:

1. Based on the epoxidation and subsequent ring opening reactions, predict which compound (A, B, C, or D) will be the final product.
2. Provide the IUPAC name of the correct starting material in Box 1.

---

**Box 1 (name):** [Your Answer Here]

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