Be sure to answer all parts. An allylic alcohol contains an OH group on a carbon atom adjacent to a C-C double bond. Treatment of allylic alcohol A with HCI forms a mixture of two allylic chlorides, B and C. Select a stepwise mechanism that illustrates how both products are formed. HCI + H,O B Part 1: Select the correct first step. :C: :C:
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.
![Be sure to answer all parts.
An allylic alcohol contains an OH group on a carbon atom adjacent to a C-C double bond. Treatment
of allylic alcohol A with HCl forms a mixture of two allylic chlorides, B and C. Select a stepwise
mechanism that illustrates how both products are formed.
HCT
+ H;O
B.
Part 1:
Select the correct first step.
:CI:
:C:
OH
ä:
HO.
OH
:CI:
HO.
Part 2 out of 4
Select all the appropriate resonance structures that result from the first step that is reproduced below.
→ resenance structures
+ H;O
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