For each of the following reactions, draw the product(s). In addition, for those reactions that have a carbocation intermediate(s), draw its structure(s). NO REACTION is possible. CH3 || CH;CHCH,ČHCH2CH CH3 [H] [0] а) Он .CCH3 [0] b) ? ČH3 CH,CH2CHCH,CH3 c) + PCI3 Он CH2CH3 H,SO4, 250°C H,SO4, 250°C d) ? + H2O - OH
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.
![Certainly! Below is a transcription of the chemical reactions presented in the image:
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**Instructions:**
For each of the following reactions, draw the product(s). In addition, for those reactions that have a carbocation intermediate(s), draw its structure(s). Note that NO REACTION is also possible.
**Reactions:**
a)
- Reactant: CH₃CHCH₂CHCH₂CH (CH₃ at carbon 2, C=O at carbon 5)
- Reagents: [H], [O]
b)
- Reactant: Aromatic ring with OH and CCH₃ groups (CCH₃ in meta position to OH)
- Reagents: [O]
c)
- Reactant: CH₃CH₂CHCH₂CH₃ (OH at carbon 3)
- Reagent: PCl₃, Δ (heat)
d)
- Reactant: Cyclohexanol (6-membered carbon ring with OH group)
- Reagent: H₂SO₄, 250°C, + H₂O
e)
- Reactants:
- CH₃CH₂CH₂CCH₃ (OH at carbon 3)
- CH₃C(OCH₂CH₂CH₃)(CH₃)
- Reagent: H₂O, Acid Catalyst
f)
- Reactants:
- CH₃CHCHCH₃ (SH at carbon 2)
- CH₃CHCHCH₃ (SH at carbon 2)
- Reagent: [O]
g)
- Reactants:
- CH₃CHCHCH₂CH₃ (C=O at carbon 3)
- CH₃CHCHCH₂CH₃ (C=O at carbon 2)
- Reagent: NaOH, Catalyst
h)
- Reactants:
- Cyclohexanone (C=O)
- CH₃CH₂CH₂OH
- Reagent: Acid Catalyst
i)
- Reactants:
- CH₃CH₂CHCH₂CH₂OH (OH at carbon 5)
- CH₃CH₂CHCH₂CH₂OH (OH at carbon 5)
- Reagent: H₂SO₄, 140°C
j)
- Reactant: CH₃](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F2c98f3ef-62be-46e3-974a-9aed57987b3e%2F4d15adce-42c4-4326-839c-4bd0b6d428ab%2Fr0ysmgq_processed.png&w=3840&q=75)
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