NEET Class 11 Chemistry MCQs – Organic Chemistry: Some Basic Principles and Techniques

Class 11 – Organic Chemistry: Some Basic Principles and Techniques (40 MCQs)

Introduction to Organic Chemistry (1–4)

  1. Organic chemistry primarily deals with compounds of:
    a) Oxygen
    b) Carbon
    c) Nitrogen
    d) Hydrogen
  2. Which of the following is an organic compound?
    a) NaCl
    b) CH₄
    c) CaCO₃
    d) H₂O
  3. Organic compounds are generally:
    a) Ionic
    b) Covalent
    c) Metallic
    d) Electrolytic
  4. Which type of bonds is most common in organic compounds?
    a) Ionic bonds
    b) Covalent bonds
    c) Hydrogen bonds
    d) Metallic bonds

Methods of Preparation of Organic Compounds (5–10)

  1. Methane can be prepared by:
    a) Wurtz reaction
    b) Reduction of CO
    c) Sabatier reaction
    d) Friedel–Crafts reaction
  2. Ethanol can be prepared by:
    a) Fermentation of sugars
    b) Hydrolysis of alkanes
    c) Oxidation of aldehydes
    d) Dehydration of carboxylic acids
  3. Which reaction is used to prepare alkyl halides?
    a) Halogenation
    b) Hydrolysis
    c) Dehydration
    d) Oxidation
  4. Which method is commonly used to prepare alkanes?
    a) Wurtz reaction
    b) Electrophilic addition
    c) Nucleophilic substitution
    d) Esterification
  5. Preparation of benzene from acetylene involves:
    a) Cyclization
    b) Halogenation
    c) Hydrogenation
    d) Dehydration
  6. Grignard reagent is prepared by:
    a) Reaction of alkyl halide with Mg in dry ether
    b) Halogenation of alkanes
    c) Oxidation of alcohols
    d) Reduction of aldehydes

Purification Techniques (11–17)

  1. Distillation is used to separate liquids based on:
    a) Density
    b) Solubility
    c) Boiling points
    d) Polarity
  2. Fractional distillation is used when boiling points differ by:
    a) >50°C
    b) <25°C
    c) 100°C
    d) 0°C
  3. Crystallization separates solids based on:
    a) Solubility
    b) Volatility
    c) Density
    d) Color
  4. Sublimation is used to purify:
    a) Soluble salts
    b) Organic solids that sublime
    c) Acids
    d) Bases
  5. Paper chromatography separates compounds based on:
    a) Molecular weight
    b) Differential solubility and adsorption
    c) Boiling point
    d) Density
  6. Thin layer chromatography (TLC) uses:
    a) Glass plates coated with adsorbent
    b) Filter paper only
    c) Distillation columns
    d) Centrifugation
  7. Purification of iodine is done by:
    a) Sublimation
    b) Filtration
    c) Distillation
    d) Chromatography

Types of Organic Reactions (18–24)

  1. CH₄ + Cl₂ → CH₃Cl + HCl is an example of:
    a) Addition
    b) Substitution
    c) Elimination
    d) Oxidation
  2. H₂C=CH₂ + H₂ → CH₃–CH₃ is an example of:
    a) Substitution
    b) Addition
    c) Elimination
    d) Polymerization
  3. C₂H₅OH → C₂H₄ + H₂O is an example of:
    a) Oxidation
    b) Reduction
    c) Elimination
    d) Substitution
  4. Oxidation of ethanol to ethanal involves:
    a) Addition
    b) Substitution
    c) Oxidation
    d) Reduction
  5. Bromination of ethene (C₂H₄) is an example of:
    a) Substitution
    b) Addition
    c) Elimination
    d) Redox
  6. Combustion of methane is:
    a) Redox reaction
    b) Substitution only
    c) Addition
    d) Elimination
  7. Esterification is an example of:
    a) Addition
    b) Substitution
    c) Condensation reaction
    d) Oxidation

Isomerism (25–31)

  1. Compounds with same molecular formula but different structures are called:
    a) Isotopes
    b) Isomers
    c) Homologues
    d) Allotropes
  2. Structural isomers differ in:
    a) Molecular formula
    b) Functional group or connectivity
    c) Physical state only
    d) Molecular weight
  3. Functional isomerism arises due to:
    a) Different carbon chain
    b) Different functional groups
    c) Different isotopes
    d) Different polarity
  4. Geometrical isomerism occurs in:
    a) Alkanes
    b) Alkenes
    c) Alkynes
    d) Alcohols
  5. Optical isomerism arises due to:
    a) Presence of chiral carbon
    b) Double bonds
    c) Triple bonds
    d) Functional group
  6. Cis–trans isomerism is a type of:
    a) Structural isomerism
    b) Geometrical isomerism
    c) Optical isomerism
    d) Functional isomerism
  7. Enantiomers are:
    a) Non-superimposable mirror images
    b) Same molecule
    c) Structural isomers
    d) Geometrical isomers

Nomenclature Basics (32–36)

  1. Prefix ‘methyl’ refers to:
    a) –CH₃
    b) –CH₂–
    c) –CH
    d) –C
  2. The IUPAC name of CH₃–CH₂–OH is:
    a) Methanol
    b) Ethanol
    c) Propanol
    d) Ethanal
  3. The parent chain is chosen based on:
    a) Longest carbon chain
    b) Shortest chain
    c) Number of functional groups only
    d) Number of hydrogens
  4. Halogen substituents are named as:
    a) Fluoro, Chloro, Bromo, Iodo
    b) Hydro, Halo, Alkyl
    c) Keto, Oxo
    d) Alkyl
  5. The functional group –COOH is named as:
    a) Alcohol
    b) Aldehyde
    c) Carboxylic acid
    d) Ketone

Conceptual & Application Questions (37–40)

  1. Organic compounds with same functional group and same general formula form:
    a) Isotopes
    b) Homologous series
    c) Geometrical isomers
    d) Optical isomers
  2. Wurtz reaction is used to prepare:
    a) Alkanes
    b) Alkenes
    c) Alkynes
    d) Alcohols
  3. Chromatography is mainly based on:
    a) Boiling points
    b) Adsorption and solubility
    c) Density
    d) Ionic character
  4. Purification of naphthalene is done by:
    a) Sublimation
    b) Crystallization
    c) Distillation
    d) Filtration

Answer Key – Class 11 Chemistry: Organic Chemistry (40 MCQs)

Introduction to Organic Chemistry (1–4)

  1. b) Carbon – Organic chemistry primarily studies carbon compounds.
  2. b) CH₄ – Methane is an organic compound.
  3. b) Covalent – Organic compounds generally contain covalent bonds.
  4. b) Covalent bonds – Most common in organic molecules.

Methods of Preparation of Organic Compounds (5–10)

  1. c) Sabatier reaction – CH₄ is prepared by hydrogenation of CO or CO₂ on nickel catalyst.
  2. a) Fermentation of sugars – Ethanol is produced biologically.
  3. a) Halogenation – Alkyl halides are prepared by substitution of H with halogen.
  4. a) Wurtz reaction – Preparation of alkanes from alkyl halides.
  5. a) Cyclization – Acetylene is converted to benzene by trimerization (cyclization).
  6. a) Reaction of alkyl halide with Mg in dry ether – Standard Grignard reagent preparation.

Purification Techniques (11–17)

  1. c) Boiling points – Distillation separates based on volatility.
  2. b) <25°C – Fractional distillation is used for close boiling liquids.
  3. a) Solubility – Crystallization separates solids based on solubility differences.
  4. b) Organic solids that sublime – Sublimation purifies substances like iodine, camphor.
  5. b) Differential solubility and adsorption – Basis of paper chromatography.
  6. a) Glass plates coated with adsorbent – TLC technique.
  7. a) Sublimation – Purification of iodine and similar solids.

Types of Organic Reactions (18–24)

  1. b) Substitution – Methane reacts with Cl₂ via substitution.
  2. b) Addition – H₂ adds to ethene across double bond.
  3. c) Elimination – Ethanol loses water to form ethene.
  4. c) Oxidation – Ethanol oxidized to ethanal.
  5. b) Addition – Bromine adds to ethene double bond.
  6. a) Redox reaction – Combustion of methane involves oxidation-reduction.
  7. c) Condensation reaction – Ester formation involves condensation of acid and alcohol.

Isomerism (25–31)

  1. b) Isomers – Same molecular formula, different structures.
  2. b) Functional group or connectivity – Structural isomerism.
  3. b) Different functional groups – Functional isomerism arises due to functional group difference.
  4. b) Alkenes – Geometrical isomerism occurs due to restricted rotation around C=C.
  5. a) Presence of chiral carbon – Optical isomerism arises from chiral centers.
  6. b) Geometrical isomerism – Cis–trans is geometrical.
  7. a) Non-superimposable mirror images – Definition of enantiomers.

Nomenclature Basics (32–36)

  1. a) –CH₃ – Methyl group.
  2. b) Ethanol – CH₃–CH₂–OH.
  3. a) Longest carbon chain – Parent chain is longest chain with functional group priority.
  4. a) Fluoro, Chloro, Bromo, Iodo – Halogen substituents.
  5. c) Carboxylic acid – –COOH functional group.

Conceptual & Application Questions (37–40)

  1. b) Homologous series – Same functional group, general formula, successive members differ by –CH₂–.
  2. a) Alkanes – Wurtz reaction couples alkyl halides to form alkanes.
  3. b) Adsorption and solubility – Basis of chromatography separation.
  4. a) Sublimation – Purification of naphthalene exploits its ability to sublime.

Disclaimer:
All MCQs on this page are created for educational purposes only. They are intended for practice and NEET/Class 11 Chemistry preparation and do not guarantee any specific exam results.