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प्रश्न
Draw a neat diagram for the following:
Haworth formula of glucopyranose.
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उत्तर

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संबंधित प्रश्न
\[\ce{CH2OH-CO-(CHOH)4-CH2OH}\] is an example of ______.
Give scientific reasons:
Hydrolysis of sucrose is called inversion.
Give two evidences for presence of formyl group in glucose.
Draw a neat diagram for the following:
Haworth formula of maltose
Write chemical reaction for following conversions
glucose into glucoxime
Classify the following carbohydrates into monosaccharide, disaccharide, oligosaccharide and polysaccharide:
glucose, cellulose, maltose, stachyose
What is the action of the following reagents on glucose?
hydroxylamine
What is the action of the following reagents on glucose?
hydrogen iodide
Define carbohydrates.
Draw the Haworth projection structure of the following.
α-D-(–)-Fructofuranose
Explain D and L configuration in sugars.
Write a chemical reaction to convert glucose into glucose cyanohydrin.
Identify the bond that links the carbon of two adjacent monosaccharides.
Identify the given structure 'P' and 'Q'.


From the following identify an example of disaccharides.
Formation of lactose by conden ation results in the release of how many molecules of water?
______ is the prosthetic group of glycoproteins.
Identify the sugar having the molecular formula C6H1206.
From the following identify the materials that are made up of cellulose.
i. Plant cell wall
ii. Exoskeleton of arthropods
iii. Paper from plant pulp
iv. Cotton fibre
Identify a non-reducing carbohydrate from the following.
Chitin is a/an ______.
____________ do not give smaller sugar units on hydrolysis.
Identify the CORRECT combination.
Match the columns and select the correct option.
| Column I | Column II | ||
| i. | Starch | a. | Animal storage molecule |
| ii. | Cellulose | b. | Plant storage molecule |
| iii. | Glycogen | c. | Heparin |
| iv. | Heteropolysaccharide | d. | Plant cell wall component |
Which carbon atoms of α- D glucopyranose and β-D-fructofuranose respectively are linked together to form glycosidic linkage in sucrose?
All these carbohydrates contain \[\ce{1 -> 4β}\] glycosidic linkage, EXCEPT ____________.
One mole of a carbohydrate on hydrolysis gives one mole of glucose and one mole of galactose. Identify the carbohydrate.
Which of the following monosaccharide is a ketohexose?
Which among the following statements is true for amylose?
Which one of the following sugar does NOT have same empirical fonnula as that of carbohydrate?
On hydrolysis sucrose gives ____________.
Identify the product Y in the following reaction.
\[\ce{Maltose ->[Hydrolysis] X ->[dil. HNO3][(excess)] Y}\]
Which one of the following rotates the plane polarized light towards left?
Which one given below is a non-reducing sugar?
Assertion: A solution of sucrose in water is dextrorotatory. But on hydrolysis in the presence of little hydrochloric acid, it becomes levorotatory.
Reason: Sucrose hydrolysis gives equal amounts of glucose and fructose. As a result of this change in sign of rotation is observed.
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
If 'n' represents total number of asymmetric carbon atoms in a compound, then the possible· number of optical isomers of the compound is ______.
Lactose is made of ______.
The two monosaccharides in a disaccharide are held together by ______ bonds.
Identify the monosaccharide containing only one asymmetric carbon atom in its molecule.
Corn is immersed in boiling water. It is then cooled, and the solution becomes sweet. It is due to ______.
Consider the following reaction
\[\ce{A <-[Br2 - H2O] Glucose ->[HNO3] B}\]
Here, 'A' and 'B' are respectively.
The glycosidic linkage present in maltose is ______.
Why carbohydrates are generally optically active.
Why carbohydrates are generally optically active?
Write Fischer projection formulae for glucose.
CH2 OH - CO - (CHOH)4 - CH2 OH is an example of ______.
\[\ce{CH2OH-CO-(CHOH)4-CH2OH}\] is an example of ______.
Why carbohydrates are generally optically active.
