
Which statements are correct?
(This question has multiple correct options)
A.Lactose is a disaccharide and is a reducing sugar
B. \[\alpha - D\] – glucopyranoside has an acetal structure and is non-reducing sugar
C.Methyl \[\alpha - D\] - glucopyranose has an acetal structure and is a non-reducing sugar
D. \[\alpha - D\] – Glucopyranose has a hemiacetal structure and is a reducing sugar
Answer
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Hint: Glucose will reduce Fehling's solution \[[Cu(II) \to Cu(I)]\left[ {Cu\left( {II} \right) \to Cu\left( I \right)} \right]\] and Tollens’s reagent \[[Ag(I) \to Ag(0)]\left[ {Ag\left( I \right) \to Ag\left( 0 \right)} \right]\] and it is thus classified as a reducing sugar.
Complete step by step answer:
A reducing sugar is any sugar that is capable of acting as a reducing agent because it has a free aldehyde group or a ketone group.
Glucose is reducing sugar because it can be oxidised by and thus reduce mild oxidising agents such as $C{u^{2 + }}$ or $A{g^ + }$ . All monosaccharides including glucose are reducing in nature.
In order for an oxidation to occur, the cyclic form must first ring-open to give the reactive aldehyde.
Hemi-acetal is a compound formed by the addition of an alcohol to an aldehyde or ketone. Any sugar that contains a hemi- acetal will be a reducing sugar. Any Glycosides which are acetal are not reducing sugars.
Lactose is a disaccharide sugar. It is also a reducing sugar composed of one molecule of D-galactose and one molecule of D-glucose found in milk joined by a \[\beta \] – 1, 4-glycosidic bond (the bond from the anomeric carbon of the first monosaccharide unit being directed upward).
\[\alpha - D\] – glucopyranoside has an acetal structure and is non-reducing sugar.
Methyl \[\alpha - D\] -glucopyranose has acetal groups and hence is not a reducing sugar as the aldehyde group is not free, and is present in the form of acetal.
\[\alpha - D\] -Glucopyranose has a hemiacetal structure and is a reducing sugar as they can be changed to open chain form with an aldehyde group.
Therefore, the correct answer is option (A), (B), (C) and (B).
Note: The glycosides which are acetal are not reducing sugar. Ketoses can also be reducing sugars because they can isomerise (a tautomerization) to aldoses.
Complete step by step answer:
A reducing sugar is any sugar that is capable of acting as a reducing agent because it has a free aldehyde group or a ketone group.
Glucose is reducing sugar because it can be oxidised by and thus reduce mild oxidising agents such as $C{u^{2 + }}$ or $A{g^ + }$ . All monosaccharides including glucose are reducing in nature.
In order for an oxidation to occur, the cyclic form must first ring-open to give the reactive aldehyde.
Hemi-acetal is a compound formed by the addition of an alcohol to an aldehyde or ketone. Any sugar that contains a hemi- acetal will be a reducing sugar. Any Glycosides which are acetal are not reducing sugars.
Lactose is a disaccharide sugar. It is also a reducing sugar composed of one molecule of D-galactose and one molecule of D-glucose found in milk joined by a \[\beta \] – 1, 4-glycosidic bond (the bond from the anomeric carbon of the first monosaccharide unit being directed upward).
\[\alpha - D\] – glucopyranoside has an acetal structure and is non-reducing sugar.
Methyl \[\alpha - D\] -glucopyranose has acetal groups and hence is not a reducing sugar as the aldehyde group is not free, and is present in the form of acetal.
\[\alpha - D\] -Glucopyranose has a hemiacetal structure and is a reducing sugar as they can be changed to open chain form with an aldehyde group.
Therefore, the correct answer is option (A), (B), (C) and (B).
Note: The glycosides which are acetal are not reducing sugar. Ketoses can also be reducing sugars because they can isomerise (a tautomerization) to aldoses.
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