Q.Complete the following reactions:
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🔒 Start your 14-day free trial to unlock the full solution →Concept understanding — Nucleophilic Substitution Reactions
Nucleophilic Addition – From Intuition to Precision
Imagine you have a molecule with a carbon–oxygen double bond — a carbonyl group (C=O). That oxygen is greedy for electrons; it pulls them away from carbon, leaving the carbon slightly positive (δ+) and the oxygen slightly negative (δ−). Now, if you bring a species that is rich in electrons (a nucleophile, meaning "nucleus-loving"), it will naturally be attracted to that electron-deficient carbon. The nucleophile attacks the carbon, the π bond breaks, and the oxygen picks up a proton (or some other electrophile) to become stable. That, in a nutshell, is nucleophilic addition.
The key idea: a nucleophile adds across a polar multiple bond (usually C=O or C≡N), breaking the π bond and forming two new sigma bonds.
The Precise Statement
Nucleophilic addition is a reaction in which a nucleophile (an electron-rich species) forms a sigma bond with an electrophilic carbon atom of a polar multiple bond (typically a carbonyl group, C=O, or a nitrile, C≡N), while the π bond breaks. The resulting intermediate then captures a proton (or another electrophile) to give a neutral product.
In general form:
RX2C=O+NuX−HX+RX2C(OH)Nu
The nucleophile (NuX−) attacks the carbonyl carbon; the oxygen becomes negatively charged; then a proton (HX+) from the medium attaches to the oxygen, yielding an alcohol.
Why It Happens – The Driving Force
The carbonyl carbon is electrophilic because:
- Oxygen is more electronegative than carbon, so the C=O bond is polarised: CXδ+=OXδ−.
- The π bond is weaker than a σ bond, so it can break relatively easily.
A nucleophile (like OHX−, CNX−, or NHX3) has a lone pair or a negative charge. It seeks positive centres. The attack forms a new σ bond, and the π electrons move entirely to oxygen, creating an alkoxide ion (RX2C−OX−). This intermediate is then quenched by a proton.
A common mistake: thinking the nucleophile attacks the oxygen. No — oxygen is already electron-rich; the nucleophile goes to the carbon because it is electron-deficient.
A Concrete Example – Addition of HCN to a Ketone
Take acetone (CHX3COCHX3) and hydrogen cyanide (HCN). In the presence of a base, CNX− (the nucleophile) attacks the carbonyl carbon:
CHX3COCHX3+CNX−CHX3C(OX−)(CN)CHX3
The alkoxide intermediate then picks up a proton from HCN (or from water) to give a cyanohydrin:
CHX3C(OX−)(CN)CHX3+HX+CHX3C(OH)(CN)CHX3
The product is acetone cyanohydrin. Notice: two new sigma bonds formed (C−CN and O−H), and the π bond is gone.
What Makes a Good Nucleophile?
Strong nucleophiles are usually negatively charged or have lone pairs:
- OHX−, CNX−, NHX2X−, CHX3OX−, HX− (from hydride reagents like NaBHX4 or LiAlHX4)
- Neutral but polarisable: NHX3, HX2O (weaker, but can add under acidic conditions) …
Why this formula?
Nucleophilic Substitution Reactions: Why the Key Formulas Hold
Nucleophilic substitution reactions are a cornerstone of organic chemistry. Instead of just memorizing the rate laws, let's understand why they arise from the molecular events.
1. The Two Main Mechanisms: A Tale of Timing
The key formulas (rate laws) for nucleophilic substitution come directly from how many molecules are involved in the rate-determining step (RDS) — the slowest step that controls the overall reaction speed.
SN1: Unimolecular — The Leaving Group Goes First
The Rate Law:
Rate=k[RX]
Why?
The reaction happens in two steps:
- Slow step (RDS): The C–X bond breaks spontaneously, forming a carbocation intermediate. Only the substrate (RX) is involved.
RXslowR++X−
- Fast step: The nucleophile (Nu−) attacks the carbocation.
R++Nu−fastRNu
Since the slow step depends only on the concentration of RX, the rate law has no dependence on [Nu−]. The nucleophile arrives after the carbocation is formed — it cannot affect the speed of the first step.
Key insight: The rate is determined by how easily the leaving group leaves, not by how fast the nucleophile attacks.
SN2: Bimolecular — Simultaneous Attack and Departure
The Rate Law:
Rate=k[RX][Nu−]
Why?
The reaction occurs in one concerted step:
- The nucleophile attacks the carbon from one side at the same time as the leaving group departs from the opposite side.
- Both RX and Nu− must collide with the correct orientation and sufficient energy.
The rate depends on the frequency of productive collisions between the two molecules. This is directly proportional to the product of their concentrations:
Rate∝[RX]×[Nu−]
Key insight: Both partners are involved in the transition state simultaneously — if either is missing, the reaction cannot proceed.
2. The Transition State: Why the Formulas Are Not Just "Given"
For SN2, the transition state has a pentavalent carbon (five bonds partially formed/broken). The energy barrier depends on steric hindrance — bulkier groups around carbon make it harder for the nucleophile to approach, which is why SN2 is favored at primary carbons. …
Concept: Reactions of aniline and benzenediazonium chloride — carbylamine reaction, reductive deamination, salt formation/sulphonation, reduction by ethanol, bromination, acetylation, and replacement of the diazonium group by −NO2.
Reasoning:
- (i) A primary aromatic amine with chloroform and alcoholic KOH undergoes the carbylamine reaction, giving the foul-smelling phenyl isocyanide.
- (ii) Hypophosphorous acid (H3PO2) reduces the diazonium salt, replacing −N2+ by −H: benzene.
- (iii) Being basic, aniline is first protonated by conc. H2SO4 to give anilinium hydrogensulphate; on strong heating (453–473 K) this salt rearranges to sulphanilic acid (p-aminobenzenesulphonic acid, largely as its zwitterion).
- (iv) Ethanol acts as a reducing agent toward the diazonium salt: the ring gets −H (benzene) while ethanol is oxidised to ethanal (CH3CHO).
- (v) The free −NH2 group activates the ring so strongly that bromine water gives 2,4,6-tribromoaniline (white precipitate) instantly.
- (vi) Acetic anhydride acetylates the nitrogen: acetanilide. …
These seven reactions cover the key transformations of aniline and benzenediazonium chloride — the carbylamine reaction, reductive deamination by H3PO2, salt formation with conc. H2SO4 (and sulphanilic acid on heating), reduction by ethanol, tribromination, acetylation, and replacement of the diazonium group by −NO2 via NaNO2/Cu.
Concept & Intuition
Aniline (C6H5NH2) is a primary aromatic amine. The lone pair on nitrogen makes it a nucleophile, a base, and a strong activator of the ring toward electrophilic substitution. The diazonium salt (C6H5N2+Cl−) is the opposite kind of species: −N2+ is an excellent leaving group (departing as N2 gas), so the diazonium group can be replaced by many other groups — the reagent decides which.
Let's go reaction by reaction.
(i) C6H5NH2+CHCl3+alc. KOH→
This is the carbylamine reaction, given only by primary amines. The amine attacks dichlorocarbene (:CCl2), generated in situ from chloroform and base; elimination of HCl then gives the isocyanide.
Product: C6H5NC (phenyl isocyanide)
(ii) C6H5N2+Cl−+H3PO2+H2O→
Hypophosphorous acid is a mild reducing agent that replaces the diazonium group by hydrogen — reductive deamination.
Product: C6H6 (benzene), with N2, H3PO3 and HCl
(iii) C6H5NH2+H2SO4 (conc.)→
Two stages, and both matter:
- Immediately (acid–base reaction): the basic amino group is protonated, giving the salt anilinium hydrogensulphate, C6H5NH3+HSO4−.
- On heating at 453–473 K: the salt rearranges (sulphonation "baking" process) to give sulphanilic acid — p-aminobenzenesulphonic acid — which exists largely as its zwitterion p-+H3N-C6H4-SO3−.
As the question prints no heating condition, the direct product of mixing is the anilinium salt; the full textbook sequence continues to sulphanilic acid on heating, and both stages should be shown.
Product: C6H5NH3+HSO4−; on heating (453–473 K) → sulphanilic acid (zwitterion)
(iv) C6H5N2+Cl−+C2H5OH→
Ethanol acts as a reducing agent here, not a nucleophile: the diazonium group is replaced by hydrogen while ethanol itself is oxidised to acetaldehyde. The net outcome parallels reaction (ii).
Product: C6H6 (benzene) + CH3CHO (ethanal)
(v) C6H5NH2+Br2(aq)→
The free −NH2 group activates the ring so powerfully that bromine water substitutes all the ortho and para positions at once — no catalyst needed.
Product: 2,4,6-tribromoaniline (white precipitate)
(vi) C6H5NH2+(CH3CO)2O→
Acetic anhydride acylates the nitrogen (N-acylation), producing acetanilide.
Product: C6H5NHCOCH3 (acetanilide / N-phenylethanamide) + CH3COOH
--- …
Here is one clear solution method for each reaction, using the Reagent–Action–Product (RAP) approach: identify the reagent's chemical role (electrophile, nucleophile, acid, reducing agent, …), predict the site of attack (the amino group or the diazonium group), then write the stable product.
(i) C6H5NH2+CHCl3+alc. KOH→
- Reagent Action: Carbylamine reaction (isocyanide test). CHCl3 + strong base generates dichlorocarbene (:CCl2).
- Step: the amine's lone pair attacks the carbene; dehydrohalogenation gives the isocyanide.
- Product: phenyl isocyanide
Final: C6H5NC
(ii) C6H5N2+Cl−+H3PO2+H2O→
- Reagent Action: reductive removal of the diazonium group. H3PO2 is a mild reducing agent.
- Step: −N2+ leaves as N2; hydrogen takes its place on the ring.
- Product: benzene
Final: C6H6
(iii) C6H5NH2+H2SO4 (conc.)→
- Reagent Action: acid–base reaction first, then sulphonation on heating.
- Step 1 (immediate): the basic −NH2 is protonated → anilinium hydrogensulphate, C6H5NH3+HSO4−.
- Step 2 (on heating at 453–473 K): the salt rearranges to sulphanilic acid (p-aminobenzenesulphonic acid, largely zwitterionic).
Final: C6H5NH3+HSO4−, which on heating at 453–473 K gives p-+H3N-C6H4-SO3− (sulphanilic acid)
(iv) C6H5N2+Cl−+C2H5OH→
- Reagent Action: reduction by ethanol. Ethanol is not acting as a nucleophile here — it donates hydrogen to the ring and is itself oxidised.
- Step: the diazonium group is replaced by −H; ethanol becomes ethanal.
- Product: benzene + acetaldehyde
Final: C6H6+CH3CHO
(v) C6H5NH2+Br2(aq)→
- Reagent Action: electrophilic aromatic substitution on a very strongly activated ring.
- Step: the free −NH2 directs and activates so strongly that all three ortho/para positions are brominated at once.
- Product: 2,4,6-tribromoaniline (white precipitate)
Final: 2,4,6-Br3C6H2NH2
(vi) C6H5NH2+(CH3CO)2O→
- Reagent Action: N-acylation (nucleophilic acyl substitution on the anhydride).
- Step: the nitrogen lone pair attacks the carbonyl carbon; one acetyl group transfers to N.
- Product: acetanilide + acetic acid
Final: C6H5NHCOCH3
(vii) C6H5N2+Cl−(i) HBF4(ii) NaNO2/Cu, Δ …
Here are the common mistakes students make with these specific reactions, along with the correct reasoning and how to avoid each.
General Mistake: Confusing Diazonium Salt Reactions
Students often mix up the conditions for replacing the diazonium group (−N2+) with different groups (Cl, Br, CN, OH, H, NO₂, F). The key is to read every reagent over the arrow — the nucleophile source and the catalyst/conditions together decide the product.
Reaction (i): C6H5NH2+CHCl3+alc. KOH→
- Common Mistake: writing a simple substitution product (e.g. C6H5NHCHCl2) or a nitrile (−CN).
- Why it's wrong: this is the carbylamine reaction (isocyanide test) — base deprotonates CHCl3 to give dichlorocarbene (:CCl2), which attacks the amine's lone pair. The product carries an −NC group, not −CN.
- ✓ Correct Product: C6H5NC (phenyl isocyanide)
Reaction (ii): C6H5N2+Cl−+H3PO2+H2O→
- Common Mistake: thinking H3PO2 is an oxidising agent, or writing a coupling product.
- Why it's wrong: H3PO2 (hypophosphorous acid) is a reducing agent — it replaces the diazonium group with a hydrogen atom.
- ✓ Correct Product: C6H6 (benzene)
Reaction (iii): C6H5NH2+H2SO4 (conc.)→
- Common Mistake: jumping straight to a sulphonation product and skipping the salt stage.
- Why it's wrong: the amine is basic, so the immediate reaction is protonation — anilinium hydrogensulphate forms first. Sulphanilic acid is the product of the subsequent heating stage (453–473 K), not of simple mixing.
- ✓ Correct Product: C6H5NH3+HSO4− first; on heating at 453–473 K it rearranges to sulphanilic acid (p-+H3N-C6H4-SO3−). Show both stages.
Reaction (iv): C6H5N2+Cl−+C2H5OH→
- Common Mistake: writing the ether C6H5OC2H5 (phenetole) or a coupling product.
- Why it's wrong: ethanol acts as a reducing agent toward the diazonium salt (milder analogue of H3PO2), replacing −N2+ by −H while being oxidised itself to acetaldehyde.
- ✓ Correct Product: C6H6 (benzene) +CH3CHO (ethanal)
Reaction (v): C6H5NH2+Br2(aq)→
- Common Mistake: writing mono-bromination (o- or p-bromoaniline).
- Why it's wrong: the free −NH2 group activates the ring so strongly that tribromination occurs instantly in bromine water — mono-bromination requires acetylating the amine first.
- ✓ Correct Product: 2,4,6-tribromoaniline (white precipitate)
Reaction (vi): C6H5NH2+(CH3CO)2O→
- Common Mistake: writing a ring-acylation (Friedel–Crafts) product.
- Why it's wrong: the nitrogen lone pair is a far better nucleophile than the ring — this is N-acylation, the standard protection reaction for aniline. …
- AP EAPCET 2026Set eng-2026-05-12-FN1 markMCQQ.In which of the following set/s reactant and reagent are correctly matched to get n-propylamine as major product? I. CH3CH2CH2Cl (1-chloropropane) ----- AgNO2,Fe/HCl II. CH3CH2Cl (chloroethane) ----- NaCN,H2/Ni III. CH3CH2CONH2 (propanamide) ----- Br2/OH− Correct answer is (A) II only (B) I, II (C) II, III (D) I, III
›Reveal solutionSolution
Two independent routes correctly build n-propylamine (nitro reduction of 1-chloropropane, and nitrile chain-extension + reduction of chloroethane); the Hofmann degradation route instead shortens the chain by one carbon, giving ethylamine.
Concept and Intuition
Three very different strategies for making primary amines are being tested, and the key discipline is to count carbons through each transformation, since some routes preserve chain length and one (Hofmann bromamide degradation) deliberately removes a carbon.
- AgNO2 vs NaNO2: nitrite is an ambident nucleophile (can attack through O or N). With the softer, more covalent silver salt AgNO2, alkylation occurs preferentially through nitrogen, giving the nitroalkane as the major product (with NaNO2, the ionic character favours O-alkylation, giving the alkyl nitrite instead). Reducing a nitroalkane (Fe/HCl) gives the primary amine with the same carbon skeleton.
- The cyanide route (NaCN, then reduction) is a classic chain-extension: the nucleophilic CN− displaces the halide, adding one carbon to the chain as a nitrile, and reducing the nitrile (H2/Ni or LiAlH4) gives a primary amine that is one carbon longer than the starting halide.
- The Hofmann bromamide degradation (Br2/OH− on an amide) is the opposite: it removes the carbonyl carbon (as it leaves via an isocyanate/carbamate intermediate that loses CO2), giving a primary amine with one carbon fewer than the starting amide.
Step-by-Step Solution
- I: CH3CH2CH2Cl (3 carbons) + AgNO2 → CH3CH2CH2NO2 (1-nitropropane, N-alkylation favoured by the covalent Ag–N bond). + Fe/HCl (reduction) → CH3CH2CH2NH2 = n-propylamine. Matches. …
- AP EAPCET 2025Set eng-2025-05-22-AN1 markMCQQ.The preferred reagent for the preparation of pure alkyl chloride from alcohol is (A) HCl+ZnCl2 (B) PCl5 (C) SOCl2 (D) PCl3
›Reveal solutionSolution
Tests why thionyl chloride, not the phosphorus halides, is the preferred reagent purely on the grounds of product purity.
Concept and Intuition
Several reagents convert R−OH→R−Cl, but "preferred for pure product" is a purity argument, not a yield argument. The reagent of choice is the one whose by-products leave the flask on their own (as gases), so no work-up/purification is needed to remove them from the alkyl chloride.
Step-by-Step Solution
- R−OH+HCl/ZnCl2→R−Cl+H2O (Lucas reagent) — works well only for tertiary/some secondary alcohols and leaves ZnCl2/water behind.
- R−OH+PCl5→R−Cl+POCl3+HCl — the by-product POCl3 is a liquid that must be removed by distillation, contaminating the crude product.
- R−OH+PCl3→R−Cl+H3PO3 — leaves phosphorous acid behind, again needing separation.
- 3R−OH+SOCl2→R−Cl+SO2↑+HCl↑ — both by-products are gases that simply bubble out, so the alkyl chloride is obtained directly in pure form with essentially no work-up. …
- AP EAPCET 2025Set eng-2025-05-23-FN1 markMCQQ.The reaction of benzene diazonium chloride with Cu and HCl is known as (A) Sandmeyer reaction (B) Etard reaction (C) Finkelstein reaction (D) Gattermann reaction
›Reveal solutionSolution
This distinguishes the Sandmeyer reaction (uses cuprous salts, e.g. Cu2Cl2/Cu2Br2) from the closely related Gattermann reaction (uses copper powder directly with HCl/HBr) for converting a diazonium salt to an aryl halide.
Concept and Intuition
Both reactions replace the diazonium group (−N2+) with a halogen via a radical/copper-mediated mechanism, and both give the same type of product (aryl halide + N2). The distinguishing feature examiners test is the reagent form: Sandmeyer's reaction historically uses a cuprous halide salt (e.g. Cu2Cl2) generated in situ or added directly, while the Gattermann reaction is the simplified variant that uses copper powder (metallic Cu) together with the corresponding hydrohalic acid (HCl/HBr) — no cuprous salt needed.
Step-by-Step Solution
- The reaction described is ArN2+Cl− treated with Cu (metal powder) and HCl.
- Because the copper source is elemental copper powder (not a cuprous salt like Cu2Cl2), this specific reagent combination is named the Gattermann reaction, distinguishing it from the Sandmeyer reaction (which specifically uses cuprous chloride/cuprous bromide). …
- AP EAPCET 2023Set ap-2023-05-23-AN1 markMCQQ.Hydrolysis products of isobutyl isonitrile are (A) (CH3)2CHCH2NH2+HCOOH (B) CH3CH2CH(CH3)NH2+HCOOH (C) (CH3)2CHNH2+CH3COOH (D) (CH3)2CHCOOH+CH3NH2
›Reveal solutionSolution
Isonitrile hydrolysis always gives the corresponding primary amine (with the SAME alkyl group as the isonitrile) plus formic acid — the alkyl group itself is never altered.
Concept and Intuition
An isocyanide, R−N≡C, is hydrolysed under acidic aqueous conditions by nucleophilic attack of water at the terminal carbon, ultimately cleaving the C–N bond to release the alkyl group AS AN AMINE (with its nitrogen intact, unchanged connectivity to R) while the isocyanide carbon (originally bonded only to N and nothing else besides the lone pair/triple bond) ends up as formic acid, HCOOH. This is a key distinguishing test reaction of isocyanides vs their isomeric nitriles (which hydrolyse differently, to carboxylic acids + ammonia/amine on the OTHER side).
Step-by-Step Solution
- Isobutyl isonitrile: (CH3)2CHCH2−N≡C — the isobutyl group ((CH3)2CHCH2−) is attached to the isocyanide nitrogen.
- Acid-catalysed hydrolysis proceeds: R−NC+2H2OH+R−NH2+HCOOH.
- Applying this to isobutyl isonitrile: the alkyl group R = (CH3)2CHCH2− ends up as the primary amine (CH3)2CHCH2NH2 (isobutylamine), retaining the exact same carbon skeleton and nitrogen attachment. …
- AP EAPCET 2022Set eng-2022-07-04-FN1 markMCQQ.When 1-chloro butane is treated with aqueous KOH it gives P. However, when it is treated with alcoholic KOH it gives Q. Identify the products P and Q respectively (A) P = CH3CH2CH2CH2OH (1-butanol), Q = CH3CH2CH2CH2OH (1-butanol) (B) P = CH2=CHCH2CH3 (but-1-ene), Q = CH3CH=CHCH3 (but-2-ene) (C) P = CH2=CHCH2CH3 (but-1-ene), Q = CH3CH2CH2CH2OH (1-butanol) (D) P = CH3CH2CH2CH2OH (1-butanol), Q = CH2=CHCH2CH3 (but-1-ene)
›Reveal solutionSolution
Aqueous KOH gives substitution (1-butanol); alcoholic KOH gives elimination, and since only C2 has beta-hydrogens, the only possible alkene is but-1-ene.
Concept and Intuition
Alkyl halides react differently depending on the solvent/base used: aqueous KOH (with water as solvent) favours SN2 nucleophilic substitution because OH− acts predominantly as a nucleophile in the polar protic medium, while alcoholic KOH (KOH dissolved in ethanol, with much less free water) favours E2 elimination, as the base character of OH−/ethoxide dominates, abstracting a beta-hydrogen to form an alkene.
Step-by-Step Solution
- Substrate: 1-chlorobutane, CH3CH2CH2CH2Cl -- a primary alkyl halide, Cl on C1.
- Aqueous KOH: favours SN2 substitution (primary halides are ideal SN2 substrates -- unhindered backside attack). OH− displaces Cl− directly: product P = CH3CH2CH2CH2OH (1-butanol).
- Alcoholic KOH: favours E2 elimination. The base removes a beta-hydrogen (a hydrogen on the carbon adjacent to the one bearing Cl).
- In 1-chlorobutane, C1 bears Cl; the only carbon adjacent to C1 is C2 -- so the only beta-hydrogens available are those on C2. There is no other beta-carbon (C1 is a terminal/primary carbon), so there is only one possible elimination direction. …
- AP EAPCET 2021Set eng-2021-08-25-AN1 markMCQQ.Identify the compound (B) in given reaction. CH3ClKCN(A)H+/H2O(B) (A) CH3NH2 (B) HCOOH (C) CH3COOH (D) CH3COCH3
›Reveal solutionSolution
CH3Cl with KCN forms methyl cyanide, and acidic hydrolysis of that nitrile gives acetic acid.
Concept and Intuition
Potassium cyanide, being an ionic (predominantly carbon-nucleophilic) source of CN−, substitutes alkyl halides via their carbon end to give alkyl cyanides (nitriles), R–C≡N, rather than isocyanides. Nitriles are the functional equivalent of a "masked carboxylic acid" — acidic (or basic) hydrolysis converts the C≡N group all the way to −COOH (via an amide intermediate).
Step-by-Step Solution
- CH3Cl+KCN→CH3CN+KCl — this is (A), methyl cyanide (acetonitrile).
- Acidic hydrolysis of a nitrile: CH3CN+2H2OH+CH3COOH+NH3 (via the amide CH3CONH2 intermediate).
- So (B)=CH3COOH (acetic acid).
Common Mistakes …
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