Sigma Percentile
JEE Main 2019
LEVELJEE Main

Animated Solution for Chemistry - Organic Chemistry: Amylopectin is composed of

Select Answer:

Visualized Solution

Structure of Amylopectin

  • Amylopectin is a highly branched polymer of glucose.
  • It is the water-soluble component of starch.

Monomeric Unit

  • The fundamental building block is -D-glucose.
  • The anomeric group at is oriented downwards.

Linear Chain Linkage

  • The main straight chain is formed by connecting of one glucose to of the next.
  • This is called an -glycosidic linkage.

Branching Linkage

  • Branching occurs when of a new glucose unit connects to of the main chain.
  • This forms an -glycosidic linkage.

Final Conclusion

  • Amylopectin consists of -D-glucose.
  • It contains both and linkages.

Comparison with Other Polysaccharides

  • Amylose: Linear chain with only linkages.
  • Glycogen: Similar to amylopectin but more highly branched.

The Sigma Insight: Biomolecules

Solution Diagram

Introduction to Starch

Starch is the primary energy storage molecule found in plants.
It is not a single compound, but rather a mixture of two distinct polysaccharides: amylose and amylopectin.
While amylose is a simple, linear chain, amylopectin is a highly branched, water-soluble polymer that makes up the bulk of starch.

The Monomer: -D-Glucose

To understand amylopectin, we must first look at its fundamental building block.
The entire polymer is constructed exclusively from -D-glucose monomers.
We can identify the -anomer by looking at the first carbon atom (the anomeric carbon). In the -configuration, the hydroxyl () group points downwards, opposite to the group on carbon-5.

Building the Backbone: -Glycosidic Linkages

The main linear backbone of amylopectin is formed by linking these glucose units end-to-end.
Specifically, the hydroxyl group on carbon-1 of one glucose molecule reacts with the hydroxyl group on carbon-4 of the adjacent molecule.
This condensation reaction releases a water molecule and forms an -glycosidic linkage. This specific bond is responsible for creating the long, straight chains of the polymer.

Branching Out: -Glycosidic Linkages

What makes amylopectin unique is its highly branched structure.
Approximately every 24 to 30 glucose units along the main chain, a new branch shoots off.
This branching occurs when carbon-1 of a new glucose unit forms a bond with the oxygen attached to carbon-6 of a glucose unit already in the main chain.
This creates the -glycosidic linkage, which serves as the critical branching point for the molecule.

Conclusion and Comparisons

By combining these structural facts, we can definitively say that amylopectin is composed of -D-glucose units connected by both and linkages.
It is highly beneficial to compare this with other polysaccharides. For instance, amylose contains only linkages, making it strictly linear.
On the other hand, glycogen (the animal equivalent of starch) possesses the exact same linkages as amylopectin but is branched much more frequently, allowing for even faster energy release!

Similar Questions

JEE Main 2021
LEVELJEE Main

Which one of the following compounds contain glycosidic linkage?

(A)
Lactose
(B)
Sucrose
(C)
Maltose
(D)
Amylose
JEE Advanced 2015
LEVELJEE Main

The structure of D-(+)-glucose is The structure of L(–)-glucose is

(A)
(B)
(C)
(D)
JEE Main 2021
LEVELJEE Main

Compound A gives D-galactose and D-glucose on hydrolysis. The compound A is

(A)
amylose
(B)
sucrose
(C)
maltose
(D)
lactose
JEE Main 2021
LEVELJEE Main

Match List-I with List-II. Choose the correct answer from the options given below.

(A)
A (i), B (iii), C (ii)
(B)
A (iii), B (i), C (iii)
(C)
A (ii), B (i), C (iii)
(D)
A (iii), B (ii), C (i)
JEE Main 2019
LEVELJEE Main

Which of the given statements is incorrect about glycogen?

(A)
It is straight chain polymer similar to amylose
(B)
Only -linkages are present in the molecule
(C)
It is present in animal cells
(D)
It is present in some yeast and fungi
JEE Main
LEVELJEE Main

Glucose and galactose are having identical configuration in all the positions except position.

(A)
C-3
(B)
C-4
(C)
C-2
(D)
C-5
JEE Advanced 2022
LEVELJEE Main

Treatment of D-glucose with aqueous NaOH results in a mixture of monosaccharides, which are

(A)
(B)
(C)
(D)
JEE Main 2019
LEVELJEE Main

Maltose on treatment with dilute HCl gives

(A)
D-glucose and D-fructose
(B)
D-fructose
(C)
D-galactose
(D)
D-glucose
JEE Main 2021
LEVELJEE Main

The secondary structure of protein is stabilised by

(A)
peptide bond
(B)
glycosidic bond
(C)
hydrogen bonding
(D)
van der Waals' forces
JEE Main 2019
LEVELJEE Main

Number of stereo-centers present in linear and cyclic structures of glucose are respectively

(A)
4 and 5
(B)
4 and 4
(C)
5 and 4
(D)
5 and 5