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NEET ChemistryUpdated 19 Oct 2026

Hydrocarbons: NEET PYQs and weightage

Hydrocarbons carries 5.9 of 100 Chemistry marks in NEET by past-paper share: 42 of the 707 tagged NEET Chemistry PYQs in the ViJEEta bank (NEET 2013–2026). It ranks 3 of 26 Chemistry chapters.

5.9/100 Weight in Chemistry
4 of 5 Exam importance (4/5, by past-paper share)
42 NEET PYQs
505 Practice questions
453 With measured difficulty

How the weight is computed: this chapter's tagged NEET PYQs divided by all tagged NEET Chemistry PYQs in the bank (42 of 707), times 100, with repeated questions counted once. The bank does not store the year of each NEET question, so none is printed. Computed from the bank at build time. Updated 19 Oct 2026.

Hydrocarbons: key facts for NEET

16 facts the paper keeps asking, each with how it is asked. Copy it onto one page of your notebook: that page is this chapter's handbook.

  1. Alkanes: formula and shape

    Alkanes are and with a tetrahedral shape: is , is and is .

    Asked as: hybridisation or bond angle of methane, or which formula belongs to the alkane series.

  2. Chain isomers of alkanes

    Chain isomers: has 2, has 3, has 5, has 9, and has 75.

    Asked as: "How many structural isomers does have?"

  3. Preparation of alkanes

    Wurtz ( in dry ether) and Kolbe electrolysis (alkane forms at the anode) both give even-carbon alkanes. Soda-lime decarboxylation gives an alkane with one carbon less.

    Asked as: methane cannot be made by Kolbe's method; the sodium salt of butanoic acid gives propane.

  4. Physical state and boiling points

    – are gases, – are liquids and are solids. Branching lowers b.p.: n-pentane isopentane neopentane .

    Asked as: arrange isomeric pentanes by boiling point (a more spherical shape means less surface contact).

  5. Halogenation of alkanes

    Halogenation is free radical (needs or heat). Halogen reactivity is , and H replacement is . Iodination is reversible and needs or .

    Asked as: why ethane forms during chlorination of methane (two radicals combine at termination).

  6. Conformations of ethane

    Staggered ethane is more stable than eclipsed ethane, with an energy gap of about . Bond angles and lengths stay the same, and the conformers cannot be isolated.

    Asked as: which conformation has maximum torsional strain, or the size of the energy barrier.

  7. Alkenes: the double bond

    Alkenes are . is one bond () plus one weaker bond (). is against for .

    Asked as: why alkenes are attacked by electrophiles (loosely held electrons).

  8. Cis-trans isomerism

    Cis-trans isomerism needs two different groups on each doubly bonded carbon. Cis-but-2-ene has and trans has , but the trans isomer has the higher m.p.

    Asked as: which compound shows geometrical isomerism; does not.

  9. Preparation of alkenes

    Lindlar's catalyst ( poisoned with sulphur compounds or quinoline) gives cis alkenes and Na in liquid gives trans alkenes. Alcoholic KOH removes HX by -elimination, with rate for the halogen and for the alkyl group.

    Asked as: match the reagent to the geometry of the product, or which alkyl halide dehydrohalogenates fastest.

  10. Markovnikov rule

    Markovnikov rule: the negative part adds to the carbon with fewer H atoms, via the more stable carbocation (for propene, the carbocation rather than the ). Propene + HBr gives 2-bromopropane. HX reactivity is .

    Asked as: the major product of HX adding to an unsymmetrical alkene.

  11. Peroxide (Kharash) effect

    The peroxide (Kharash) effect gives anti-Markovnikov addition by a free radical path. Propene + HBr + benzoyl peroxide gives 1-bromopropane.

    Asked as: "Peroxide effect is shown by: HCl / HBr / HI?"

  12. Tests for unsaturation and ozonolysis

    Two tests for unsaturation: reddish-orange in is decolourised, and cold dilute aqueous (Baeyer's reagent) gives vicinal glycols. Ozonolysis ( followed by ) locates the double bond.

    Asked as: identify the alkene from its ozonolysis products, e.g. ethanal + pentan-3-one.

  13. Alkynes: the triple bond

    Alkynes are . Ethyne is -hybridised, linear (), with at and , made of 1 and 2 bonds. gives ethyne.

    Asked as: arrange , and by bond length or bond enthalpy.

  14. Acidity of terminal alkynes

    Terminal alkyne H atoms are acidic because carbon has s character, so they react with Na or . Acidity runs , and ethyne ethene ethane.

    Asked as: which alkyne does not form a sodium salt (but-2-yne).

  15. Benzene and aromaticity

    In benzene all bonds are , between single () and double (). The ring is planar and , with 6 delocalised electrons. Aromaticity needs planarity, complete delocalisation and electrons (Hückel).

    Asked as: which ring is aromatic, or why benzene prefers substitution to addition.

  16. Directive influence of substituents

    Directive influence: , , and are o/p-directing and activating. Halogens are o/p-directing but deactivating. , , , and are meta-directing.

    Asked as: rank substituted benzenes by reactivity toward (toluene benzene m-dinitrobenzene).

Trap

The peroxide effect works only with HBr. With HCl, the H–Cl bond (430.5 kJ mol⁻¹) is too strong for the free radical to break. With HI, iodine radicals join to form I₂ instead of adding to the double bond. So HCl and HI always follow Markovnikov, even when peroxide is present.

How does NEET ask Hydrocarbons?

8 real previous-year questions from this chapter, as printed in the paper, each with its worked solution. Answer the first one here with no sign-in.

Q1ChemistryNEET UG PYQPreparation of Alkanes
Try right here · No sign-in
Which of the following alkane cannot be made in good yield by Wurtz reaction?
Answer key (A) & worked solution

Correct answer: Option A

Wurtz reaction is used to prepare symmetrical alkane.
Q2ChemistryNEET UG PYQPreparation of Alkanes
Hydrocarbon (A) reacts with bromine by substitution to form an alkyl bromide which by Wurtz reaction is converted to gaseous hydrocarbon containing less than four carbon atoms. (A) is
ACH – CH
BCH = CH
CCH ≡ CH
DCH
Answer key (D) & worked solution

Correct answer: Option D

Hence the correct option is (4)
Q3ChemistryNEET UG PYQChemical Properties of Alkenes
Which of the following statements are NOT correct? A. Hydrogen is used to reduce heavy metal oxides to metals. B. Heavy water is used to study reaction mechanism. C. Hydrogen is used to make saturated fats from oils D. The bond dissociation enthalpy is lowest as compared to a single bond between two atoms of any element. E. Hydrogen reduces oxides of metals that are more active than iron. Choose the most appropriate answer from the options given below:
AB, D only
BD, E only
CA, B, C only
DB, C, D, E only
Answer key (B) & worked solution

Correct answer: Option B

(D, E) explanation (D) bond strength/ bond dissociation energy/bond energy of can not be lowest because bond formed between hydrogen atoms is due to overlapping of . (E) Hydrogen can not reduces oxides of highly reactive metal.
Q4ChemistryNEET UG PYQChemical Properties of Alkanes
Methane reacts with steam at 1273 K in the presence of nickel catalyst to form :
ACO and
BCO and
C and
D and
Answer key (A) & worked solution

Correct answer: Option A

(Used for industrial preparation of dihydrogen gas)
Q5ChemistryNEET UG PYQChemical Properties of Aromatic Hydrocarbons
Which of the following compounds will not undergo Friedal-Craft’s reaction easily?
ACumene
BXylene
CNitrobenzene
DToluene
Answer key (C) & worked solution

Correct answer: Option C

-NO is a deactivating group, and therefore, nitrobenzene will not undergo Friedal-Crafts reaction.
Q6ChemistryNEET UG PYQChemical Properties of Alkynes
Which one is the correct order of acidity?
ACHCH > CH = CH > CH – CCH > CH – CH.
BCH – CH > CH = CH > CH – CCH > CHCH
CCH = CH CH – C CH > CHCH
DCHCH > CH – C CH > CH = CH > CH – CH
Answer key (D) & worked solution

Correct answer: Option D

Correct order is
Q7ChemistryNEET UG PYQPhysical Properties of Alkanes
Given below are two statements: Statement I: The boiling point of three isomeric pentanes follows the order n-pentane > isopentane > neopentane Statement II: When branching increases, the molecule attains a shape of sphere. This results in smaller surface area for contact, due to which the intermolecular forces between the spherical molecules are weak, thereby lowering the boiling point. In the light of the above statements, choose the most appropriate answer from the options given below:
ABoth statement I and statement II are incorrect
BStatement I is correct but statement II is incorrect
CStatement I is incorrect but statement II is correct
DBoth statement I and statement II are correct
Answer key (D) & worked solution

Correct answer: Option D

Branching increases boiling point decreases Pentane, 309.1 K Isopentane, 300.9 K Neopentane, 282.9 K Option (d) is correct
Q8ChemistryNEET UG PYQChemical Properties of Aromatic Hydrocarbons
Some meta-direction substituents in aromatic substitution are given. Which one is most deactivating ?
A
B–SOH
C-COOH
D–NO
Answer key (D) & worked solution

Correct answer: Option D

-NOis the most deactivating.

Which topics in Hydrocarbons carry the most questions?

The 12 busiest of 26 topics, by tagged PYQs, then practice questions. Counted from the bank. Updated 19 Oct 2026.

TopicPYQsPractice questions
Chemical Properties of Alkenes15163
Chemical Properties of Aromatic Hydrocarbons1098
Chemical Properties of Alkynes446
Preparation of Alkanes430
Chemical Properties of Alkanes240
Preparation of Alkynes113
Physical Properties of Alkanes111
Introduction and Classification of Hydrocarbons19
Nomenclature of Hydrocarbons18
Preparation of Aromatic Hydrocarbons17
Structure of Alkenes16
Isomerism in Alkenes15

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