b) Write the products of your compound and the following reagents. If the reaction would not work well for your compound write "NR" and explain what the problem would be. NaCN H* HOCH,CH,OH H* H_NNHC H (CH₂),P=CHCH₂CH₂CH₂ LiCu(CH₂CH3)2 CH,MgBr Cro, H₂O*
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.
![# Organic Chemistry Problem Set
## Problem 1
Consider the compound depicted below:
![Hexagon with a double bond O on top, a CH2O group on the left with a solid wedge, and an H group with a dashed wedge on the same carbon]
### Part a
**Task:**
- Provide the IUPAC name for the compound, incorporating stereochemistry indicators such as cis/trans, E/Z, and R/S where applicable.
### Part b
**Instructions:**
- Write the products formed when "your compound" reacts with each of the following reagents. If a reaction is unsuitable for "your compound," indicate this with "NR" (No Reaction) and specify what the issue would be.
1. **Reagent: NaCN**
- Reaction: ——————>
2. **Reagent: \(H^+\)**
- Reaction: ——————>
3. **Reagent: HOCH\(_2\)CH\(_2\)OH**
- Reaction: ——————>
4. **Reagent: \(H^+\)**
- Reaction: ——————>
5. **Reagent: \(H_2NNHC_6H_5\)**
- Reaction: ——————>
6. **Reagent: (C\(_6\)H\(_5\))\(_3\)P=CHCH\(_2\)CH\(_3\)**
- Reaction: ——————>
7. **Reagent: LiCu(CH\(_2\)CH\(_3\))\(_2\)**
- Reaction: ——————>
8. **Reagent: CH\(_3\)MgBr followed by \(H_2O^+\)**
- Reaction: ——————>
9. **Reagent: CrO\(_3\)**
- Reaction: ——————>](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F1932ea18-1310-44c1-b1da-825fb09ef63f%2F1887be67-69ed-49bf-8526-06ac4c663a50%2F8b6nkyt_processed.jpeg&w=3840&q=75)
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