JEE Chemistry Purification And Characterisation Of Organic Compounds MCQs Set 01

Multiple Choice Questions (MCQs) for JEE Chemistry: Purification And Characterisation Of Organic Compounds

Access targeted multiple-choice questions for Purification And Characterisation Of Organic Compounds designed to align with the latest JEE academic syllabus for JEE Chemistry. These objective practice sets help students evaluate their conceptual understanding and improve exam readiness.

Practice Purification And Characterisation Of Organic Compounds MCQs for JEE Chemistry

Access the complete set of multiple-choice questions for Purification And Characterisation Of Organic Compounds below. This focused format allows students to isolate specific topics for thorough review and uninterrupted practice alongside official JEE textbooks.

Multiple Choice Questions

Question 1: A compound contains C = 90% and H = 10%. Its empirical formula is
(a) \( \ce{C3H10} \)
(b) \( \ce{CH2} \)
(c) \( \ce{C3H2} \)
(d) \( \ce{C3H4} \)
Show Answer & Explanation

Answer: (d) \( \ce{C3H4} \)

Explanation:
1. Moles: C = 90/12 = 7.5, H = 10/1 = 10
2. Ratio C : H = 7.5 : 10 = 3 : 4

Teacher's Note:
1. Convert every percentage or mass to moles first and divide by the smallest value to get the simplest ratio.
2. Check the answer by recomputing the formula mass and comparing it with the given molecular mass.

Question 2: An organic compound on analysis gave C = 48 g, H = 8 g and N = 56 g. The volume of 1.0 g of the compound at NTP is 200 mL. Its molecular formula is
(a) \( \ce{C4H8N4} \)
(b) \( \ce{C2H4N2} \)
(c) \( \ce{C12H24N12} \)
(d) \( \ce{C16H32N16} \)
Show Answer & Explanation

Answer: (a) \( \ce{C4H8N4} \)

Explanation:
1. Molar mass = 22400/200 = 112 g/mol
2. Moles: C = 48/12 = 4, H = 8, N = 56/14 = 4, so the ratio is CH2N
3. Mass of CH2N = 12 + 2 + 14 = 28, and 112/28 = 4, giving \( \ce{C4H8N4} \)

Teacher's Note:
1. Use the standard factor method: the fraction of the element in the weighed product times its mass gives the mass of the element.
2. Divide by the mass of the sample and multiply by 100 for the percentage.

Question 3: Insulin contains 3.4% sulphur. The minimum molecular weight of insulin is
(a) 350
(b) 470
(c) 560
(d) 940
Show Answer & Explanation

Answer: (d) 940

Explanation:
1. Each molecule must contain at least one S atom (32 u)
2. Minimum molar mass = 32 x 100/3.4 = 941, i.e. about 940

Teacher's Note:
1. Convert every percentage or mass to moles first and divide by the smallest value to get the simplest ratio.
2. Check the answer by recomputing the formula mass and comparing it with the given molecular mass.

Question 4: On complete combustion, 1.4 g of a hydrocarbon gave 1.8 g of water. The empirical formula of the hydrocarbon is
(a) \( \ce{CH} \)
(b) \( \ce{CH2} \)
(c) \( \ce{CH3} \)
(d) \( \ce{CH4} \)
Show Answer & Explanation

Answer: (b) \( \ce{CH2} \)

Explanation:
1. H in 1.8 g of water = 1.8 x 2/18 = 0.2 g
2. C = 1.4 - 0.2 = 1.2 g, so moles C = 0.1 and H = 0.2
3. Ratio 1 : 2 gives \( \ce{CH2} \)

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Question 5: In the estimation of sulphur in an organic compound, the sulphur is converted by conc. \( \ce{HNO3} \) (Carius method) into
(a) \( \ce{SO2} \)
(b) \( \ce{H2S} \)
(c) \( \ce{H2SO4} \)
(d) \( \ce{SO3} \)
Show Answer & Explanation

Answer: (c) \( \ce{H2SO4} \)

Explanation:
1. Fuming nitric acid oxidises the sulphur of the compound to sulphuric acid
2. Barium chloride then precipitates it as \( \ce{BaSO4} \) for weighing

Teacher's Note:
1. Match the technique to the property that differs between the components: boiling point, solubility, volatility or adsorption.
2. Questions often ask why one method is chosen over another.

Question 6: 0.24 g of an organic compound gave 0.22 g of \( \ce{CO2} \) on complete combustion. If it contains 1.66% hydrogen, the percentages of carbon and oxygen are respectively
(a) 12.5 and 36.6
(b) 25 and 73.3
(c) 25 and 36.6
(d) 25 and 80
Show Answer & Explanation

Answer: (b) 25 and 73.3

Explanation:
1. C in 0.22 g \( \ce{CO2} \) = 12/44 x 0.22 = 0.06 g, so % C = 0.06/0.24 x 100 = 25
2. % O = 100 - 25 - 1.66 = 73.3 (the compound contains only C, H and O)

Teacher's Note:
1. Convert every percentage or mass to moles first and divide by the smallest value to get the simplest ratio.
2. Check the answer by recomputing the formula mass and comparing it with the given molecular mass.

Question 7: An organic compound contains C = 74.0%, H = 8.65% and N = 17.3%. Its empirical formula is
(a) \( \ce{C5H8N} \)
(b) \( \ce{C10H12N} \)
(c) \( \ce{C5H7N} \)
(d) \( \ce{C10H14N} \)
Show Answer & Explanation

Answer: (c) \( \ce{C5H7N} \)

Explanation:
1. Moles: C = 74/12 = 6.17, H = 8.65, N = 17.3/14 = 1.24
2. Dividing by 1.24 gives 5 : 7 : 1, so \( \ce{C5H7N} \)

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Question 8: The molecular weight of an organic acid is given by
(a) Equivalent weight x basicity
(b) Equivalent weight / basicity
(c) Basicity / equivalent weight
(d) Equivalent weight x valency
Show Answer & Explanation

Answer: (a) Equivalent weight x basicity

Explanation:
1. Equivalent weight = molecular weight / basicity
2. Hence molecular weight = equivalent weight x basicity

Teacher's Note:
1. Use the standard factor method: the fraction of the element in the weighed product times its mass gives the mass of the element.
2. Divide by the mass of the sample and multiply by 100 for the percentage.

Question 9: If two compounds have the same empirical formula but different molecular formulae, they must have
(a) Different percentage composition
(b) Different molecular weight
(c) Same viscosity
(d) Same vapour density
Show Answer & Explanation

Answer: (b) Different molecular weight

Explanation:
1. Same empirical formula means the same percentage composition
2. Molecular formula = (empirical formula) x n with different n, so the molecular weights differ (and so do the vapour densities)

Teacher's Note:
1. Convert every percentage or mass to moles first and divide by the smallest value to get the simplest ratio.
2. Check the answer by recomputing the formula mass and comparing it with the given molecular mass.

Question 10: 60 g of a compound on analysis gave C = 24 g, H = 4 g and O = 32 g. Its empirical formula is
(a) \( \ce{C2H4O2} \)
(b) \( \ce{C2H2O} \)
(c) \( \ce{CH2O2} \)
(d) \( \ce{CH2O} \)
Show Answer & Explanation

Answer: (d) \( \ce{CH2O} \)

Explanation:
1. Moles: C = 24/12 = 2, H = 4, O = 32/16 = 2
2. Ratio 1 : 2 : 1 gives \( \ce{CH2O} \)

Teacher's Note:
1. Use the standard factor method: the fraction of the element in the weighed product times its mass gives the mass of the element.
2. Divide by the mass of the sample and multiply by 100 for the percentage.

Question 11: An organic compound contains C = 38.8%, H = 16% and N = 45.2%. Its empirical formula is
(a) \( \ce{CH3NH2} \)
(b) \( \ce{CH3CN} \)
(c) \( \ce{C2H5CN} \)
(d) \( \ce{CH2(NH)2} \)
Show Answer & Explanation

Answer: (a) \( \ce{CH3NH2} \)

Explanation:
1. Moles: C = 3.23, H = 16, N = 3.23
2. Ratio 1 : 5 : 1 gives \( \ce{CH5N} \), which is \( \ce{CH3NH2} \)

Teacher's Note:
1. Convert every percentage or mass to moles first and divide by the smallest value to get the simplest ratio.
2. Check the answer by recomputing the formula mass and comparing it with the given molecular mass.

Question 12: An organic compound gave C = 54.5%, O = 36.4% and H = 9.1%. Its empirical formula is
(a) \( \ce{CH3O} \)
(b) \( \ce{C2H4O} \)
(c) \( \ce{C3H4O} \)
(d) \( \ce{C4H8O} \)
Show Answer & Explanation

Answer: (b) \( \ce{C2H4O} \)

Explanation:
1. Moles: C = 4.54, O = 2.28, H = 9.1
2. Dividing by 2.28 gives C : H : O = 2 : 4 : 1

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Question 13: An organic compound gave C = 92.31% and H = 7.69%. If its molecular weight is 78, the molecular formula is
(a) \( \ce{C6H6} \)
(b) \( \ce{C7H7} \)
(c) \( \ce{C6H18} \)
(d) \( \ce{C8H20} \)
Show Answer & Explanation

Answer: (a) \( \ce{C6H6} \)

Explanation:
1. Moles: C = 7.69, H = 7.69, so the empirical formula is \( \ce{CH} \) (mass 13)
2. n = 78/13 = 6, so the molecular formula is \( \ce{C6H6} \)

Teacher's Note:
1. Use the standard factor method: the fraction of the element in the weighed product times its mass gives the mass of the element.
2. Divide by the mass of the sample and multiply by 100 for the percentage.

Question 14: A compound gave 80% carbon and 20% hydrogen on analysis. The compound is possibly
(a) \( \ce{C6H6} \)
(b) \( \ce{C2H5OH} \)
(c) \( \ce{C2H6} \)
(d) \( \ce{CHCl3} \)
Show Answer & Explanation

Answer: (c) \( \ce{C2H6} \)

Explanation:
1. Moles: C = 6.67, H = 20, ratio 1 : 3 giving \( \ce{CH3} \)
2. Doubling gives the saturated hydrocarbon \( \ce{C2H6} \) (ethane)

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Question 15: A compound has 50% carbon and 50% oxygen by mass and an approximate molecular weight of 290. Its molecular formula is
(a) \( \ce{CO} \)
(b) \( \ce{C4O3} \)
(c) \( \ce{C12O9} \)
(d) \( \ce{C3O3} \)
Show Answer & Explanation

Answer: (c) \( \ce{C12O9} \)

Explanation:
1. Moles: C = 4.17, O = 3.125, ratio 4 : 3 so the empirical formula is \( \ce{C4O3} \) (mass 112)
2. 290/112 = 2.6, nearest whole number 3 gives \( \ce{C12O9} \) (mass 288)

Teacher's Note:
1. Use the standard factor method: the fraction of the element in the weighed product times its mass gives the mass of the element.
2. Divide by the mass of the sample and multiply by 100 for the percentage.

Question 16: An organic compound has C = 60%, H = 13.3% and O = 26.7%. Its empirical formula is
(a) \( \ce{C3H6O} \)
(b) \( \ce{C2H6O2} \)
(c) \( \ce{C4H8O2} \)
(d) \( \ce{C3H8O} \)
Show Answer & Explanation

Answer: (d) \( \ce{C3H8O} \)

Explanation:
1. Moles: C = 5, H = 13.3, O = 1.67
2. Dividing by 1.67 gives 3 : 8 : 1

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Question 17: 64 g of an organic compound contains 24 g of carbon, 8 g of hydrogen and the rest oxygen. Its empirical formula is
(a) \( \ce{CH2O} \)
(b) \( \ce{C2H4O} \)
(c) \( \ce{CH4O} \)
(d) \( \ce{C2H8O2} \)
Show Answer & Explanation

Answer: (c) \( \ce{CH4O} \)

Explanation:
1. O = 64 - 24 - 8 = 32 g
2. Moles C = 2, H = 8, O = 2, so the ratio is 1 : 4 : 1

Teacher's Note:
1. Convert every percentage or mass to moles first and divide by the smallest value to get the simplest ratio.
2. Check the answer by recomputing the formula mass and comparing it with the given molecular mass.

Question 18: An organic compound contains C, H and O in the ratio 6 : 1 : 8 by weight. Its vapour density is 30. Its molecular formula is
(a) \( \ce{C2H4O2} \)
(b) \( \ce{CH4O} \)
(c) \( \ce{CH2O} \)
(d) \( \ce{C3HO} \)
Show Answer & Explanation

Answer: (a) \( \ce{C2H4O2} \)

Explanation:
1. Moles: C = 6/12 = 0.5, H = 1, O = 8/16 = 0.5, so the empirical formula is \( \ce{CH2O} \) (30)
2. Molecular mass = 2 x 30 = 60, n = 2, giving \( \ce{C2H4O2} \)

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Question 19: The empirical formula of a hydrocarbon containing 80% carbon and 20% hydrogen is
(a) \( \ce{CH} \)
(b) \( \ce{CH2} \)
(c) \( \ce{CH3} \)
(d) \( \ce{CH4} \)
Show Answer & Explanation

Answer: (c) \( \ce{CH3} \)

Explanation:
1. Moles: C = 6.67, H = 20
2. Ratio 1 : 3

Teacher's Note:
1. Convert every percentage or mass to moles first and divide by the smallest value to get the simplest ratio.
2. Check the answer by recomputing the formula mass and comparing it with the given molecular mass.

Question 20: An organic compound with C = 40% and H = 6.7% has the empirical formula
(a) \( \ce{CH2} \)
(b) \( \ce{CH2O} \)
(c) \( \ce{C3H6O3} \)
(d) \( \ce{C2H4O2} \)
Show Answer & Explanation

Answer: (b) \( \ce{CH2O} \)

Explanation:
1. O = 100 - 40 - 6.7 = 53.3%
2. Moles C = 3.33, H = 6.7, O = 3.33, ratio 1 : 2 : 1; the empirical formula is the simplest ratio, \( \ce{CH2O} \)

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Question 21: An organic compound containing C, H and N gave C = 40%, H = 13.33% and N = 46.67%. Its empirical formula is
(a) \( \ce{C2H7N2} \)
(b) \( \ce{CH5N} \)
(c) \( \ce{CH4N} \)
(d) \( \ce{C2H7N} \)
Show Answer & Explanation

Answer: (c) \( \ce{CH4N} \)

Explanation:
1. Moles: C = 3.33, H = 13.33, N = 3.33
2. Ratio 1 : 4 : 1

Teacher's Note:
1. Convert every percentage or mass to moles first and divide by the smallest value to get the simplest ratio.
2. Check the answer by recomputing the formula mass and comparing it with the given molecular mass.

Question 22: A compound contains C = 18.5%, H = 1.55%, Cl = 55.04% and O = 24.81%. Its empirical formula is
(a) \( \ce{CHClO} \)
(b) \( \ce{CH2ClO} \)
(c) \( \ce{C2H2OCl} \)
(d) \( \ce{ClCH2O} \)
Show Answer & Explanation

Answer: (a) \( \ce{CHClO} \)

Explanation:
1. Moles: C = 1.54, H = 1.55, Cl = 55.04/35.5 = 1.55, O = 1.55
2. The ratio is 1 : 1 : 1 : 1

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Question 23: 0.2595 g of an organic substance gave 0.35 g of barium sulphate in a quantitative analysis. The percentage of sulphur in the substance is
(a) 18.52
(b) 182.2
(c) 17.5
(d) 175.2
Show Answer & Explanation

Answer: (a) 18.52

Explanation:
1. S in 0.35 g \( \ce{BaSO4} \) = 32/233 x 0.35 = 0.0481 g
2. % S = 0.0481/0.2595 x 100 = 18.52

Teacher's Note:
1. Convert every percentage or mass to moles first and divide by the smallest value to get the simplest ratio.
2. Check the answer by recomputing the formula mass and comparing it with the given molecular mass.

Question 24: In Kjeldahl's method, \( \ce{CuSO4} \) acts as
(a) Oxidising agent
(b) Reducing agent
(c) Hydrolysing agent
(d) Catalytic agent
Show Answer & Explanation

Answer: (d) Catalytic agent

Explanation:
1. \( \ce{CuSO4} \) (with \( \ce{K2SO4} \)) is added to the digestion mixture
2. It speeds up the conversion of nitrogen to ammonium sulphate and so acts as a catalyst

Teacher's Note:
1. Learn each test with its observation and the compound responsible for the colour or precipitate.
2. Remember which method suits which kind of sample (volatile, non-volatile, heat-sensitive).

Question 25: An organic compound has C = 10.06%, H = 0.84% and Cl = 89.10%. If its vapour density is 60, the molecular formula is
(a) \( \ce{CH2Cl2} \)
(b) \( \ce{CHCl3} \)
(c) \( \ce{CH3Cl} \)
(d) None of these
Show Answer & Explanation

Answer: (b) \( \ce{CHCl3} \)

Explanation:
1. Moles: C = 0.84, H = 0.84, Cl = 2.51, ratio 1 : 1 : 3
2. Empirical mass 119.5; molecular mass = 2 x 60 = 120, so \( \ce{CHCl3} \)

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Question 26: The percentage of nitrogen in urea is about
(a) 18.05
(b) 28.29
(c) 46.66
(d) 85.56
Show Answer & Explanation

Answer: (c) 46.66

Explanation:
1. Urea is \( \ce{CO(NH2)2} \), molar mass 60
2. % N = 28/60 x 100 = 46.67

Teacher's Note:
1. Use the standard factor method: the fraction of the element in the weighed product times its mass gives the mass of the element.
2. Divide by the mass of the sample and multiply by 100 for the percentage.

Question 27: Which of the following is the best test for the presence of water in a liquid?
(a) Use of anhydrous copper sulphate
(b) Use of litmus paper
(c) Taste
(d) Smell
Show Answer & Explanation

Answer: (a) Use of anhydrous copper sulphate

Explanation:
1. White anhydrous \( \ce{CuSO4} \) turns blue on forming the pentahydrate
2. Litmus only indicates acidity or basicity, and taste and smell are unsafe and non-specific

Teacher's Note:
1. Learn each test with its observation and the compound responsible for the colour or precipitate.
2. Remember which method suits which kind of sample (volatile, non-volatile, heat-sensitive).

Question 28: To differentiate between carbon-12, carbon-13 and carbon-14, the instrument used is a
(a) Infra-red spectrometer
(b) Atomic absorption spectrometer
(c) Mass spectrometer
(d) Ultraviolet spectrometer
Show Answer & Explanation

Answer: (c) Mass spectrometer

Explanation:
1. The three isotopes differ in mass
2. A mass spectrometer separates ions according to the mass-to-charge ratio

Teacher's Note:
1. Match the technique to the property that differs between the components: boiling point, solubility, volatility or adsorption.
2. Questions often ask why one method is chosen over another.

Question 29: An organic compound has the empirical formula \( \ce{CH2O} \) and a molecular weight of 90. Its molecular formula is (C = 12, H = 1, O = 16)
(a) \( \ce{C3H6O3} \)
(b) \( \ce{C2H6O2} \)
(c) \( \ce{C2H2O} \)
(d) \( \ce{CH2O} \)
Show Answer & Explanation

Answer: (a) \( \ce{C3H6O3} \)

Explanation:
1. Empirical mass = 30, n = 90/30 = 3
2. Molecular formula = \( \ce{C3H6O3} \)

Teacher's Note:
1. Write the working as mass of element, then moles, then ratio. This avoids slips with atomic masses.
2. Round only when a ratio is within about 0.1 of a whole number.

Multiple Choice Questions (MCQs) for JEE Chemistry Purification And Characterisation Of Organic Compounds

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