The Haworth projection shown below represents | vedclass

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(D) The given structure is a six-membered ring containing an oxygen atom,which identifies it as a pyranose form.In the Haworth projection of $D$-gluco

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$\alpha-D-(+)-$ Glucopyranose

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(D) The given structure is a six-membered ring containing an oxygen atom,which identifies it as a pyranose form.In the Haworth projection of $D$-glucose,the anomeric carbon $(C1)$ has the $-OH$ group pointing downwards,which corresponds to the $\alpha-$configuration.The other hydroxyl groups at $C2, C3,$ and $C4$ are arranged such that they match the structure of $D$-glucose.Specifically,the $-OH$ at $C2$ is down,at $C3$ is up,and at $C4$ is down.Therefore,the structure represents $\alpha-D-(+)-$ glucopyranose.

List-$I$ (Glycosidic linkage)	List-$II$ (Polysaccharide)
$A$. $\alpha-1,4$	$I$. Amylose
$B$. $\beta-1,4$	$II$. Cellulose
$C$. $\alpha-1,4, \alpha-1,6$	$III$. Amylopectin

The Haworth projection shown below represents:

Similar Questions

Which of the following reduces Tollens' reagent?

Which of the following is invert sugar?

$D$-Glucose $\overset{OH^{-}}{\longleftrightarrow} A + B$; $A$ and $B$ are

Match the following:
List-$I$ (Glycosidic linkage) List-$II$ (Polysaccharide)
$A$. $\alpha-1,4$ $I$. Amylose
$B$. $\beta-1,4$ $II$. Cellulose
$C$. $\alpha-1,4, \alpha-1,6$ $III$. Amylopectin

Identify the given structure:

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