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प्रश्न
Draw the structure of α-D glucopyranose.
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उत्तर

संबंधित प्रश्न
\[\ce{CH2OH-CO-(CHOH)4-CH2OH}\] is an example of ______.
Glucose on oxidation with dilute nitric acid gives _______________
Write the name of the unit to which glucose unit is linked to from sucrose.
Explain the preparation of glucose from sucrose.
Write chemical reaction for following conversions
glucose into glucoxime
Explain the classification of carbohydrates with examples.
What is the action of the following reagents on glucose?
hydroxylamine
Write a commercial method for preparation of glucose.
What is monosaccharide?
Identify the given structure 'P' and 'Q'.


From the following identify an example of disaccharides.
Identify the substances having glycosidic bond and peptide bond, respectively in their structure:
Formation of lactose by conden ation results in the release of how many molecules of water?
From the following identify the group that is exclusively consists of polysaccharides.
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.
Identify the CORRECT combination.
Prolonged heating of glucose with hot HI results in the formation of ____________.
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 one of the following is an oligosaccharide?
Which one of the following is NOT soluble in water?
Which following reagent is used to detect presence of five hydroxyl groups in a glucose molecule?
Which one of the following sugar does NOT have same empirical fonnula as that of carbohydrate?
How many moles of fructose and galactose respectively are obtained on hydrolysis of 1 mole stachyose?
What is the number of hydroxyl groups present in lactic acid?
Identify the number of secondary carbon atoms in glucose.
Which among the following reagents is used to confirm the presence of carbonyl group in glucose?
On hydrolysis sucrose gives ____________.
Which among the following sugars does not reduce Tollen's reagent?
Identify the number of oxygen atoms present in saccharic acid?
Which among the following reagents is used to obtain gluconic acid from glucose?
Identify the product Y in the following reaction.
\[\ce{Maltose ->[Hydrolysis] X ->[dil. HNO3][(excess)] Y}\]
How many moles of acetic acid are obtained in the reaction when one mole glucose is treated with excess acetic anhydride?
When one mole of lactose is hydrolysed, the hydrolysate contains ____________.
Which one given below is a non-reducing sugar?
\[\ce{Glucose ->[(HCN)] Product ->[(hydrolysis)] Product ->[(HI + Heat)] A}\], the compound A is:
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.
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.
Maltose
Write the structure of α-D (+) glucopyranose.
Which of the following groups contain polysaccharides?
A molecule of stachyose contains how many carbon atoms?
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 |
Formation of gluconic acid from glucose by oxidation using Br2 water.
Consider the following reaction
\[\ce{A <-[Br2 - H2O] Glucose ->[HNO3] B}\]
Here, 'A' and 'B' are respectively.
\[\ce{CH2OH - CO - (CHOH)4 - CH2OH}\] is an example of ______.
Explain the hydrolysis of sucrose.
Why carbohydrates are generally optically active.
Why carbohydrates are generally optically active.
Why carbohydrates are generally optically active?
Why carbohydrates are generally optically active?
What are the number of chiral carbon atoms and the number of formyl groups, respectively, present in ribose?
