Multiple Choice
A D-aldopentose is subjected to Kiliani-Fischer chain lengthening. What products result?
A) two aldohexoses which are epimeric at C3
B) two enantiomeric aldohexoses
C) two enantiomeric aldopentoses
D) two aldohexoses which are epimeric at C2
E) a D-aldohexose and an L-aldohexose
Correct Answer:

Verified
Correct Answer:
Verified
Q83: Draw the structure of D-glyceraldehyde.
Q84: Compound X is a cyclic six-carbon monosaccharide.
Q85: Provide the structure of the open-chain form
Q86: All chiral D-sugars rotate plane-polarized light _.<br>A)
Q87: What is the major structural difference between
Q89: Soyasaponin is a natural product found in
Q90: What is the result of reaction involving
Q91: Stereoisomeric aldohexoses that differ in configuration at
Q92: What is the major organic product of
Q93: What are the two most common unwanted