6) Write a mechanism for the conversion of compound 1 to compound 4. In going from compound 1-4 in Schemel, why does the OH- attacks that particular ring and carbon as opposed to the double bonds in the other rings or other carbons in the center ring. Need to bear in mind that charged molecules are unstable and nature favors neuralization of charges. OH OH ト HO red OOH O-glucose compound 1 O-glucose OH colorless OH HO O-glucose compound 4 O-glucose OH

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Chapter1: Chemical Foundations
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6) Write a mechanism for the conversion of compound 1 to compound 4. In going from
compound 1-4 in Schemel, why does the OH- attacks that particular ring and carbon as
opposed to the double bonds in the other rings or other carbons in the center ring. Need
to bear in mind that charged molecules are unstable and nature favors neuralization of
charges.
OH
OH
ト
HO
red
OOH
O-glucose
compound 1
O-glucose
OH
colorless
OH
HO
O-glucose
compound 4
O-glucose
OH
Transcribed Image Text:6) Write a mechanism for the conversion of compound 1 to compound 4. In going from compound 1-4 in Schemel, why does the OH- attacks that particular ring and carbon as opposed to the double bonds in the other rings or other carbons in the center ring. Need to bear in mind that charged molecules are unstable and nature favors neuralization of charges. OH OH ト HO red OOH O-glucose compound 1 O-glucose OH colorless OH HO O-glucose compound 4 O-glucose OH
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