Carbohydrates: Structures and Functions

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33 Questions

What are the main uses of carbohydrates?

Source of energy and structural components

What is the molar ratio of carbohydrates in terms of carbon, hydrogen, and oxygen?

C1H2O1

Which type of carbohydrate can be categorized as a simple building block?

Monosaccharides

What determines how two sugars interact when forming a bond in disaccharides?

Anomeric carbon

What type of bond is formed between the anomeric carbon of maltose?

Alpha (1-4) bond

Which group attacks the aldehyde group to form an intramolecular hemiacetal group in the formation of cyclic glucose?

Hydroxyl group

In which position does the OH group point when the alcohol group attacks the aldehyde from the top in the formation of cyclic glucose?

Equatorial position

What is the main property of enantiomers?

Same chemical formula and mirror images

How can D glucose be identified based on its penultimate carbon?

Hydroxyl pointing right

Which test is used to detect reducing sugars like glucose in a sample?

Benedict’s test

What color does starch turn when iodine is added to it?

Blue-black

What type of glycosylation occurs on amino acids serine and threonine?

O-linked glycosylation

What is the composition of starch?

Amylose and amylopectin

What type of linkage does cellulose have between glucose units?

Beta 1-4 linkage

Which type of bond does glycogen have at its branching points?

Alpha 1-6 glycosidic linkages

Which type of test is used to detect for the presence of starch?

Iodine test

What is the result of the alcohol group attacking the aldehyde from the top in the formation of cyclic glucose?

The OH group points across in an equatorial position

What is the composition of starch?

Both amylose and amylopectin with different glycosidic bonds

Which type of glycosylation occurs on amino acids serine and threonine?

O-linked glycosylation

What is the main property of enantiomers?

They are mirror images of each other

What determines how two sugars interact when forming a bond in disaccharides?

The chirality of the anomeric carbon

What color does starch turn when iodine is added to it?

Blue-black

What type of bond does glycogen have at its branching points?

Alpha 1-6 glycosidic bond

Which test is used to detect reducing sugars like glucose in a sample?

Benedict's test

In which position does the OH group point when the alcohol group attacks the aldehyde from the back in the formation of cyclic glucose?

Axial position pointing down

What type of linkage does cellulose have between glucose units?

Beta 1-4 linkages

Why are disaccharide bond types drawn differently?

To indicate the orientation and shape of the bond between the two disaccharides

What determines the labeling of carbons in hexoses?

The number of hydrogens attached to each carbon

What dictates how two sugars interact when forming a bond in disaccharides?

The anomeric carbon of the sugars

In which form can any carbohydrate exist?

Both cyclic and linear forms

What type of bond does glycogen have at its branching points?

Alpha-1,6-glycosidic bond

What are the main uses of carbohydrates?

Source of energy and structural components

which form of carbohydrates is favoured?

cyclic

Study Notes

Carbohydrate Properties and Structure

  • Carbohydrates have various uses, including providing energy, forming structures, and serving as markers for cell recognition.
  • The general molar ratio of carbohydrates is CH2O, with varying Carbon:Hydrogen:Oxygen ratios depending on the specific carbohydrate.

Simple Carbohydrate Building Blocks

  • Monosaccharides, such as glucose, are simple building blocks of carbohydrates.

Disaccharide Formation

  • The type of bond formed between the anomeric carbon of maltose is an α-1,4-glycosidic bond.
  • The orientation of the OH group determines how two sugars interact when forming a bond in disaccharides.

Cyclic Glucose Formation

  • In the formation of cyclic glucose, the hydroxymethyl group attacks the aldehyde from the top, resulting in a hemiacetal ring.
  • The OH group points downwards when the alcohol group attacks the aldehyde from the top.

Properties of Enantiomers

  • Enantiomers have the main property of being non-superimposable mirror images of each other.

Identifying D-Glucose

  • D-glucose can be identified based on its penultimate carbon.

Detecting Reducing Sugars

  • The Benedict's test is used to detect reducing sugars like glucose in a sample.

Starch Properties

  • Starch turns blue-black when iodine is added to it.
  • Starch is composed of long chains of α-glucose units linked by α-1,4-glycosidic bonds.

Glycosylation

  • O-glycosylation occurs on amino acids serine and threonine.

Cellulose and Glycogen Structure

  • Cellulose has β-1,4-glycosidic linkages between glucose units.
  • Glycogen has α-1,4-glycosidic linkages between glucose units, with α-1,6-glycosidic bonds at its branching points.

Detecting Starch and Glycogen

  • Iodine test is used to detect the presence of starch.

Test your knowledge about the structures and functions of carbohydrates, including their role as a source of energy, structural components, and attachment to proteins. Learn about the different types of carbohydrates and their simple building blocks.

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