#3 - The alkyl halide shown here can undergo multiple reaction pathways. Draw the two major products when this compound is treated with NaOCH3. Be sure to clearly show the stereochemistry using the dash/wedge notation where appropriate! Hint: one will be a substitution product and one will be an elimination product. CI H CH2CH3
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.
![#3 - The alkyl halide shown here can
undergo multiple reaction pathways. Draw
the two major products when this
compound is treated with NaOCH3. Be sure
to clearly show the stereochemistry using
the dash/wedge notation where
appropriate! Hint: one will be a
substitution product and one will be an
elimination product.
CI
H.
CH2CH3](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F2f591c64-216a-4120-ac44-1b23dfa641af%2Fb77ac717-0082-441f-8500-cb4278c76071%2F3zm5kx_processed.jpeg&w=3840&q=75)
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