Match the sugars in column I with their types given in column II and mark the appropriate choice.
Column I
Column II
(A) Glucose
(i) Ketohexose
(B) Fructose
(ii) Aldohexose
(C) Ribose
(iii) Aldotetrose
(D) Erythrose
(iv) Aldopentose
A
(A) → (iv), (B) → (i), (C) → (iii), (D) → (ii)
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B
(A) → (iii), (B) → (iv), (C) → (i), (D) → (ii)
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C
(A) → (i), (B) → (ii), (C) → (iii), (D) → (ii)
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D
(A) → (ii), (B) → (i), (C) → (iv), (D) → (iii)
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Solution
The correct option is D (A) → (ii), (B) → (i), (C) → (iv), (D) → (iii)
An aldohexose is a hexose with an aldehyde group on one end. The aldohexoses have four chiral centres for a total of 16 possible aldohexose stereoisomers (24). Of these, only three commonly occur in nature: D-glucose, D-galactose, and D-mannose.
A ketohexose is a ketone-containing hexose (a six-carbon monosaccharide). The most common ketohexoses, each of which represents a pair of enantiomers (D- and L-isomers), include psicose, fructose, sorbose, and tagatose.
Ribose is an aldopentose, which means a pentose sugar with an aldehyde functional group in position one
Erythrose is a tetrose saccharide with the chemical formula C4H8O4. It has one aldehyde group, and so is part of the aldose family.