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Correct answer: Anomers differ in their stereochemistry only at the anomeric carbon (C-1).
Anomers are cyclic sugar isomers that differ in configuration only at C-1 (the anomeric carbon). Alpha and beta forms of D-glucopyranose are the classic example. Both can be crystallised as pure forms, and when either pure anomer is dissolved in water it undergoes mutarotation — a gradual change in optical rotation until equilibrium is reached. All four statements are therefore correct.