When carbon disulfide (CS2) is treated with an alcohol in the presence of base, the product is a xanthate salt. If an alkyl halide is also present, a xanthate ester is formed. Propose a mechanism for each of these reactions. ROH R. O. NaOH SNa A xanthate salt S=C=S ROH/R'Br R' NaOH A xanthate ester の=O
When carbon disulfide (CS2) is treated with an alcohol in the presence of base, the product is a xanthate salt. If an alkyl halide is also present, a xanthate ester is formed. Propose a mechanism for each of these reactions. ROH R. O. NaOH SNa A xanthate salt S=C=S ROH/R'Br R' NaOH A xanthate ester の=O
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Chapter1: Chemical Foundations
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![When carbon disulfide (CS2) is treated with an alcohol in the presence of base, the product is a xanthate salt. If an alkyl
halide is also present, a xanthate ester is formed. Propose a mechanism for each of these reactions.
ROH
R.
O.
NaOH
SNa
A xanthate salt
S=C=S
ROH/R'Br
R'
NaOH
A xanthate ester
の=O](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F4d35e7d5-559b-456b-b43a-ba8ff2859fc3%2F1dc7efbb-4643-4b91-bfa7-7bc0bc782572%2Fi0hvat9.png&w=3840&q=75)
Transcribed Image Text:When carbon disulfide (CS2) is treated with an alcohol in the presence of base, the product is a xanthate salt. If an alkyl
halide is also present, a xanthate ester is formed. Propose a mechanism for each of these reactions.
ROH
R.
O.
NaOH
SNa
A xanthate salt
S=C=S
ROH/R'Br
R'
NaOH
A xanthate ester
の=O
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