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महाराष्ट्र राज्य शिक्षण मंडळएचएससी विज्ञान (सामान्य) इयत्ता १२ वी

Explain D and L configuration in sugars.

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प्रश्न

Explain D and L configuration in sugars.

थोडक्यात उत्तर
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उत्तर

D and L configuration in sugars:

  1. Conventionally (+)-glyceraldehyde is represented by the Fischer projection formula having –OH group attached to C-2 on the right side and this configuration is denoted by symbol ‘D’.
  2. Similarly, the configuration of (–) glyceraldehyde is denoted by the symbol ‘L’.
  3. All the compounds which can be correlated by a series of chemical reactions to (+)-glyceraldehyde are said to have D-configuration.
  4. And compounds which are chemically correlated to (–)-glyceraldehyde are said to have L-configuration. This is the system of the relative configuration of chiral compounds.
  5. A monosaccharide is assigned D/L configuration on the basis of the configuration of the lowest chiral carbon in its Fischer projection formula.
  6. Relative configuration of (+)-glucose with respect to (+)-glyceraldehyde can be drawn as follows:
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पाठ 14: Biomolecules - Short Answer Questions (Type-II)

व्हिडिओ ट्यूटोरियलVIEW ALL [2]

संबंधित प्रश्‍न

Give two evidences for presence of formyl group in glucose.


Explain the preparation of glucose from sucrose.


Write chemical reaction for following conversions

glucose into glucoxime


Classify the following carbohydrates into monosaccharide, disaccharide, oligosaccharide and polysaccharide:

glucose, cellulose, maltose, stachyose


Draw the Haworth projection structure of the following.

α-D-(–)-Fructofuranose


Write a chemical reaction to convert glucose into glucose cyanohydrin.


Which of the following type of carbohydrates cannot be hydrolyzed?


From the following identify an example of disaccharides.


Which enzymes would work sequentially on potatoes consumed by an individual?


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


Fructose is the fruit sugar and chemically it is ketohexose but it has a ______ rather than a ______.


Which among the following compounds is obtained when glucose reacts with hydrogen cyanide?


Identify a non-reducing carbohydrate from the following.


Which is the product obtained, when Br2 water reacts with glucose?


Match the Column I and Column II select the correct option.

  Column I   Column II
i. Monosaccharides a. Stored energy in animals
ii. Glycogen b. Polymer made from ß-glucose molecules
iii. Cellulose c. Exoskeleton of arthropods
iv. Chitin d. Building blocks of carbohydrates
    e. Plant hormone

From the following identify the two types of glucose polymers present in starch.


Which reagent among the following is used to confirm presence of aldehydic carbonyl group in glucose?


Raffinose, sucrose and stachyose are respectively ____________.


Identify the INCORRECT statement regarding glucose.


Which one of the following is an oligosaccharide?


The general formula for polysaccharide is ____________.


\[\ce{CH3 - CH2 - CH2 - Br ->[Na][dry ether] A ->[Cl2] B}\]

Identify the product B in the above reaction.


Which one of the following is Tetrose sugar? 


Which one of the following is NOT soluble in water?


Which of the following statements is NOT true for glyceraldehyde?


Which one of the following sugar does NOT have same empirical fonnula as that of carbohydrate?


Which among the following reagents is used to confirm the presence of carbonyl group in glucose?


Which of the following statement is NOT true about saccharic acid?


Which among the following reagents is used to obtain gluconic acid from glucose?


Which among the following is a product of hydrolysis of one mole raffinose?


How many hydroxyl groups are present in Erythrulose?


Which among the following observations suggests that glucose also exists in cyclic form?


The correct corresponding order of names of four aldoses with configuration given below Respectively is:


Which one given below is a non-reducing sugar?


\[\ce{Glucose ->[(HCN)] Product ->[(hydrolysis)] Product ->[(HI + Heat)] A}\], the compound A is:


The number of sp2 and sp3 hybridised carbon in fructose are respectively ____________.


Complete hydrolysis of cellulose gives ____________.


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


What are reducing and non-reducing sugars?


Classify the following into monosaccharides, oligosaccharides and polysaccharides.

Starch


Classify the following into monosaccharides, oligosaccharides and polysaccharides.

Sucrose


Is the following sugar, D-sugar or L-sugar?


Lactose is made of ______.


A molecule of stachyose contains how many carbon atoms?


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

 


Which carbon atoms of fructose are bonded together through oxygen forming fructofuranose?


Match the Column I with Column II and choose the correct answer from options below:

Column I Column II
A. Purine 1. Glycogen
B. Pyrimidine 2. Cellulose
C. Structural polysaccharide 3. Glucagon
D. Storage polysaccharide 4. Adenine
  5. Cytosine

Which one is a non-reducing commercial sugar?


The glycosidic linkage present in maltose is ______.


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


Why carbohydrates are generally optically active.


Why carbohydrates are generally optically active.


Describe the action of the following reagent on glucose:

dil. Nitric acid.


Carbohydrates that do not undergo hydrolysis further are called ______.


Write the ring structure of glucose.


What are the number of chiral carbon atoms and the number of formyl groups, respectively, present in ribose?


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