Practice MCQs for JEE Chemistry Biomolecules
Review structured MCQ sets for JEE Chemistry Biomolecules. Built according to official JEE guidelines, these downloadable questions support daily revision and core concept reinforcement.
Access Biomolecules Questions and Solutions
View or download the dedicated Biomolecules MCQ resource below. Practicing these 50 objective questions regularly builds familiarity with standard exam patterns and helps secure higher marks in final Chemistry evaluations.
Multiple Choice Questions
(a) (i), (ii) and (iii)
(b) (ii) and (iii)
(c) (i) and (iii)
(d) (i) and (ii)
Show Answer & Explanation
Answer: (d) (i) and (ii)
Explanation:
1. Denaturation destroys secondary and tertiary structure, so (i) is true.
2. DNA denaturation separates the two strands, so (ii) is true.
3. The primary structure remains intact, so (iii) is false.
Teacher's Note:
1. Only weak forces break during denaturation.
2. Peptide bonds stay unchanged.
(a) alpha-D-glucose and alpha-D-glucose
(b) alpha-D-glucose and alpha-D-fructose
(c) alpha-D-glucose and alpha-D-galactose
(d) alpha-D-fructose and alpha-D-galactose
Show Answer & Explanation
Answer: (a) alpha-D-glucose and alpha-D-glucose
Explanation:
1. Maltose is made of two alpha-D-glucose units linked through C1 to C4 alpha-glycosidic bond.
2. Hydrolysis with maltase gives only glucose.
Teacher's Note:
1. Maltose is malt sugar, a reducing sugar.
2. It is produced by the hydrolysis of starch.
(a) right, left, left, right
(b) left, left, right, right
(c) left, right, left, right
(d) right, left, right, right
Show Answer & Explanation
Answer: (d) right, left, right, right
Explanation:
1. The aldehyde group of D-glucose becomes CH=NOH. The stereocentres are untouched.
2. D-Glucose has OH groups at C-2 right, C-3 left, C-4 right and C-5 right.
3. So the oxime shows right, left, right, right.
Teacher's Note:
1. Remember the order for D-glucose as R, L, R, R from top to bottom.
2. Epimers differ at one of these positions.
(a) alpha-D-glucose and alpha-D-glucose
(b) alpha-D-glucose and beta-D-glucose
(c) alpha-D-glucose and beta-D-fructose
(d) alpha-D-glucose and alpha-D-galactose
Show Answer & Explanation
Answer: (a) alpha-D-glucose and alpha-D-glucose
Explanation:
1. Maltose has two alpha-D-glucopyranose units joined by an alpha-1,4 glycosidic link.
Teacher's Note:
1. Starch gives maltose on partial hydrolysis.
2. Maltose is a reducing sugar.
(a) sugar, phosphate and vitamin A
(b) sugar, phosphate and bases
(c) nucleic acid, vitamins and sugar
(d) sugar, amino acid and phosphate
Show Answer & Explanation
Answer: (b) sugar, phosphate and bases
Explanation:
1. Each nucleotide has a sugar, a phosphate and a nitrogenous base.
2. These units form the polynucleotide chain.
Teacher's Note:
1. Nucleoside is sugar plus base.
2. Nucleotide is nucleoside plus phosphate.
(a) the sugar in RNA is arabinose and in DNA is 2-deoxyribose
(b) the sugar in RNA is ribose and in DNA is 2-deoxyribose
(c) the sugar in RNA is arabinose
(d) the sugar in RNA is 2-deoxyribose and in DNA is arabinose
Show Answer & Explanation
Answer: (b) the sugar in RNA is ribose and in DNA is 2-deoxyribose
Explanation:
1. RNA contains ribose and DNA contains 2-deoxyribose.
2. Arabinose is not found in either.
Teacher's Note:
1. Deoxy means lacking the OH at C-2.
2. RNA is single stranded, DNA is double stranded.
(a) Maltose
(b) Lactose
(c) Glucose
(d) Sucrose
Show Answer & Explanation
Answer: (d) Sucrose
Explanation:
1. Sucrose has no free hemiacetal group because both anomeric carbons are in the glycosidic bond.
2. The others are reducing.
Teacher's Note:
1. Non-reducing sugars do not reduce Tollens' or Fehling's.
2. They also do not show mutarotation.
(a) DNA to RNA to proteins
(b) DNA to RNA to carbohydrates
(c) amino acids to proteins to DNA
(d) DNA to carbohydrates to proteins
Show Answer & Explanation
Answer: (a) DNA to RNA to proteins
Explanation:
1. DNA is transcribed into m-RNA, and m-RNA is translated into protein.
Teacher's Note:
1. Reverse transcription in retroviruses is an exception.
2. The dogma was proposed by Francis Crick.
(a) 2-amino-6-oxopurine (2-amino-6-hydroxypurine)
(b) 6-aminopurine
(c) 2,6-diaminopurine
(d) 5-methyl-2,4-dioxopyrimidine
Show Answer & Explanation
Answer: (a) 2-amino-6-oxopurine (2-amino-6-hydroxypurine)
Explanation:
1. Guanine is a purine base with an amino group at C-2 and a keto (oxo) group at C-6.
2. 6-Aminopurine is adenine, and 5-methyl-2,4-dioxopyrimidine is thymine.
Teacher's Note:
1. Purines (adenine, guanine) have a fused two-ring skeleton.
2. Pyrimidines (cytosine, thymine, uracil) have a single six-membered ring.
(a) 60
(b) 20
(c) 15
(d) 40
Show Answer & Explanation
Answer: (b) 20
Explanation:
1. Proteins in the human body are built from 20 different alpha-amino acids.
2. Four bases form 64 triplet codons, which code for these 20 amino acids and the stop signals.
Teacher's Note:
1. The number of amino acids is not four.
2. The code is degenerate, so several codons code for one amino acid.
(a) amylopectin has 1,4 alpha-linkages and 1,6 alpha-linkages
(b) amylose has 1,4 alpha-linkages and 1,6 beta-linkages
(c) amylopectin has 1,4 alpha-linkages and 1,6 beta-linkages
(d) amylose is made up of glucose and galactose
Show Answer & Explanation
Answer: (a) amylopectin has 1,4 alpha-linkages and 1,6 alpha-linkages
Explanation:
1. Amylose is a linear chain with only 1,4 alpha links.
2. Amylopectin is branched with 1,4 alpha links in the chains and 1,6 alpha links at the branch points.
3. So the statement in option (a) is correct.
Teacher's Note:
1. Both are polymers of alpha-D-glucose.
2. The 1,6 links make amylopectin branched.
(a) Aniline
(b) Acetanilide
(c) Benzoic acid
(d) Glycine
Show Answer & Explanation
Answer: (d) Glycine
Explanation:
1. A zwitterion needs both an acidic group and a basic group in the same molecule.
2. Glycine has COOH and NH2, so it exists as +NH3CH2COO-.
Teacher's Note:
1. Aniline has only a basic group and benzoic acid only an acidic group.
2. Zwitterions are why amino acids have high melting points.
(a) Fructose is a reducing sugar
(b) Cellulose is a polymer of beta-D-(+)-glucose
(c) DNA is a polymer of D-ribose
(d) Amylopectin is insoluble in water
Show Answer & Explanation
Answer: (c) DNA is a polymer of D-ribose
Explanation:
1. DNA is a polymer of nucleotides containing 2-deoxy-D-ribose, not D-ribose.
2. The other statements are correct.
Teacher's Note:
1. D-ribose is the sugar in RNA.
2. Cellulose is made of beta-1,4 linked glucose units.
(a) Tryptophan, lysine, histidine
(b) Serine, lysine, tryptophan
(c) Serine, histidine, tryptophan
(d) Serine, histidine, lysine
Show Answer & Explanation
Answer: (a) Tryptophan, lysine, histidine
Explanation:
1. Tryptophan, lysine and histidine cannot be made in the body in sufficient amounts and must be taken in the diet.
2. Serine is non-essential.
Teacher's Note:
1. Serine appears in options b, c and d, so those are all wrong.
2. Learn the list of essential amino acids once.
(a) Glucose contains an aldehyde group but does not give Schiff's test
(b) Glucose does not react with sodium hydrogen sulphite and ammonia
(c) The pentaacetate of glucose does not react with hydroxylamine, showing the absence of the -CHO group
(d) All of these
Show Answer & Explanation
Answer: (d) All of these
Explanation:
1. All three observations suggest that the aldehyde group in glucose is not free.
2. They are explained by the cyclic hemiacetal structure.
Teacher's Note:
1. Cyclic structure also explains mutarotation and the existence of anomers.
2. Glucose has a six-membered pyranose ring.
(a) 5 and 3
(b) 1 and 5
(c) 5 and 5
(d) 3 and 3
Show Answer & Explanation
Answer: (a) 5 and 3
Explanation:
1. The phosphate joins the 5 position of one sugar to the 3 position of the next sugar.
2. This repeats along the chain.
Teacher's Note:
1. Hence DNA chains have a 5 to 3 direction.
2. C-1 carries the base and is not used.
(a) It is an aldohexose
(b) On heating with HI it forms n-hexane
(c) It is present in furanose form
(d) It does not give Schiff's test
Show Answer & Explanation
Answer: (c) It is present in furanose form
Explanation:
1. Glucose is an aldohexose (a), and prolonged heating with HI gives n-hexane, showing a straight chain of six carbons (b).
2. It exists mainly in the pyranose (six-membered) form, not furanose.
3. It also fails Schiff's test (d).
Teacher's Note:
1. Fructose is the one that mainly exists in the furanose form in disaccharides.
2. Glucose forms a pyranose ring.
(a) Maltose
(b) Lactose
(c) Sucrose
(d) Cellobiose
Show Answer & Explanation
Answer: (c) Sucrose
Explanation:
1. Sucrose is made by linking the anomeric carbons of glucose and fructose.
2. No free hemiacetal group is left, so it does not reduce Tollens' or Fehling's reagent.
3. Maltose, lactose and cellobiose are reducing.
Teacher's Note:
1. A glycosidic link at both anomeric carbons makes a sugar non-reducing.
2. Trehalose is another non-reducing disaccharide.
(a) C-2 of one unit and C-4 of the other
(b) C-1 of one unit and C-2 of the other
(c) C-1 of one unit and C-4 of the other
(d) C-2 of one unit and C-3 of the other
Show Answer & Explanation
Answer: (c) C-1 of one unit and C-4 of the other
Explanation:
1. Maltose has an alpha-1,4-glycosidic bond.
2. The anomeric C-1 of one glucose joins the C-4 hydroxyl of the second glucose.
Teacher's Note:
1. The second glucose keeps a free C-1, so maltose is reducing.
2. Cellobiose has a beta-1,4 bond.
(a) Natural starch has approximately 10 to 20 percent amylose and 80 to 90 percent amylopectin
(b) Amylose is water soluble and gives a blue colour with iodine
(c) Amylopectin is a branched-chain polysaccharide, insoluble in water, and does not give the blue colour with iodine
(d) Starch is not hydrolysed by the enzyme amylase present in saliva
Show Answer & Explanation
Answer: (d) Starch is not hydrolysed by the enzyme amylase present in saliva
Explanation:
1. Salivary amylase starts the hydrolysis of starch to maltose, so (d) is incorrect.
2. Statements a, b and c are the standard facts about starch.
Teacher's Note:
1. Amylose gives deep blue with iodine, and amylopectin gives a purple-red colour.
2. Digestion of starch begins in the mouth.
(a) Proteins are high molecular mass complex biopolymers of amino acids present in all living cells
(b) Proteins may contain phosphorus and iodine
(c) Proteins may contain iron, copper, zinc and manganese
(d) All of these
Show Answer & Explanation
Answer: (d) All of these
Explanation:
1. Proteins are polymers of amino acids and occur in all cells.
2. Phosphoproteins (casein) contain phosphorus, thyroglobulin contains iodine, and metalloproteins contain iron, copper, zinc or manganese.
3. So all statements are true.
Teacher's Note:
1. Conjugated proteins have non-protein parts.
2. Haemoglobin, haemocyanin and carbonic anhydrase are examples.
Free study material for Chemistry
Practice MCQs for JEE Chemistry Biomolecules
About Biomolecules MCQs for JEE Chemistry
Test your conceptual understanding of Biomolecules with these targeted multiple-choice questions. Designed in alignment with the latest JEE curriculum for JEE Chemistry, these problem sets build accuracy and prepare students for objective exams.
How to Verify Your MCQ Answers
Cross-reference your completed choices with comprehensive NCERT solutions for JEE Chemistry to ensure absolute clarity across all sub-topics in this chapter.
Enhance Speed with Online MCQ Tests
Follow up your worksheet practice by attempting the interactive online Chemistry MCQ test for this chapter to evaluate your execution speed. All platform resources are free to access.
FAQs
You can get most exhaustive JEE Chemistry Biomolecules MCQs Set 06 for free on StudiesToday.com. These MCQs for JEE Chemistry are updated for the 2026-27 academic session as per JEE examination standards.
Yes, our JEE Chemistry Biomolecules MCQs Set 06 include the latest type of questions, such as Assertion-Reasoning and Case-based MCQs. 50% of the JEE paper is now competency-based.
By solving our JEE Chemistry Biomolecules MCQs Set 06, JEE students can improve their accuracy and speed which is important as objective questions provide a chance to secure 100% marks in the Chemistry.
Yes, Chemistry MCQs for JEE have answer key and brief explanations to help students understand logic behind the correct option as its important for 2026 competency-focused JEE exams.
Yes, you can also access online interactive tests for JEE Chemistry Biomolecules MCQs Set 06 on StudiesToday.com as they provide instant answers and score to help you track your progress in Chemistry.