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
Chemistry
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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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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