English

Draw the structure of α-D glucopyranose. - Chemistry

Advertisements
Advertisements

Question

Draw the structure of α-D glucopyranose.

Diagram
Advertisements

Solution

shaalaa.com
Biomolecules in the Cell > Carbohydrates
  Is there an error in this question or solution?
Chapter 14: Biomolecules - Very Short Answer Questions

APPEARS IN

SCERT Maharashtra Chemistry [English] 12 Standard HSC
Chapter 14 Biomolecules
Very Short Answer Questions | Q 2

RELATED QUESTIONS

Give two evidences for presence of formyl group in glucose.


Draw a neat diagram for the following:

Haworth formula of glucopyranose.


Write chemical reaction for following conversions

glucose into gluconic acid


What is the action of the following reagents on glucose?

acetic anhydride


By which of the following process formation of glycosidic bond occurs?


Which of the following monosaccharides is a tetrose sugar?


Which of the following is the basic unit of carbohydrates?


Formation of lactose by conden ation results in the release of how many molecules of water?


Identify the sugar having the molecular formula C6H1206.


Which element among the following is not present in saccharine?


Which one of the following carbohydrates is insoluble in water?


How many moles of fructose and galactose respectively are obtained on hydrolysis of 1 mole stachyose?


On hydrolysis sucrose gives ____________.


Identify the product Y in the following reaction.

\[\ce{Maltose ->[Hydrolysis] X ->[dil. HNO3][(excess)] Y}\]


How many hydroxyl groups are present in Erythrulose?


Which one of the following rotates the plane polarized light towards left?


Glucose is an aldose. Which one of the following reactions is not expected with glucose?


Classify the following into monosaccharides, oligosaccharides and polysaccharides.

Maltose


The two monosaccharides in a disaccharide are held together by ______ bonds.

 


Identify the monosaccharide containing only one asymmetric carbon atom in its molecule.


Consider the following reaction

\[\ce{A <-[Br2 - H2O] Glucose ->[HNO3] B}\]

Here, 'A' and 'B' are respectively.


Why carbohydrates are generally optically active.


Why carbohydrates are generally optically active?


Carbohydrates that do not undergo hydrolysis further are called ______.


Why carbohydrates are generally optically active.


\[\ce{CH2OH - CO - (CHOH)4 - CH2 OH}\] is an example of ______.


Why carbohydrates are generally optically active?


Why carbohydrates are generally optically active?


\[\ce{CH2OH - CO - (CHOH)4 - CH2OH}\] is an example of ______.


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×