FBISE Class 9th (SSC-l)

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FBISE Class 9th (SSC-l)

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A. A nitrile
B. A cyanohydrin (2-hydroxybutanenitrile)
C. An amide
D. An oxime
Answer: HCN adds across the C=O bond of propanal: the CN- attacks the carbonyl carbon and H+ protonates the oxygen, forming a cyanohydrin.
A. 4
B. 6
C. 8
D. 2
Answer: In a tetrahedral complex, the metal is surrounded by 4 ligands at the corners of a tetrahedron, giving a coordination number of 4.
A. KMnO4
B. SOCl2 (thionyl chloride)
C. Na2Cr2O7
D. NaOH
Answer: SOCl2 converts alcohols to alkyl chlorides with inversion of configuration (if chiral). The byproducts SO2 and HCl are gases, driving the reaction forward.
A. [Ar] 3d4 4s2
B. [Ar] 3d5 4s1
C. [Ar] 3d6 4s0
D. [Ar] 3d3 4s2 4p1
Answer: Chromium is an exception: one 4s electron promotes to 3d to achieve the extra stability of half-filled d-orbitals, giving [Ar] 3d5 4s1.
A. Free radical mechanism coupling alkyl halides
B. Nucleophilic substitution
C. Electrophilic addition
D. Elimination
Answer: The Wurtz reaction uses sodium metal to couple two alkyl halide molecules via a free radical mechanism: 2R-X + 2Na -> R-R + 2NaX.
A. -0.4 Delta_o
B. -1.6 Delta_o + 2P
C. -2.4 Delta_o + 3P
D. -0.8 Delta_o
Answer: Low-spin d6: t2g6 eg0. CFSE = 6(-0.4 Delta_o) + 0(+0.6 Delta_o) = -2.4 Delta_o, with 3 pairing energies (P) required for pairing all six electrons in t2g.
A. Pentanedial
B. Glutaraldehyde (pentanedial)
C. Cyclopentanone
D. Pentanoic acid
Answer: Ozonolysis cleaves the C=C double bond. Reductive workup (Zn/H2O or DMS) of cyclopentene gives pentanedial (glutaraldehyde), a dialdehyde with 5 carbons.
A. sp
B. sp2
C. sp3
D. sp3d
Answer: Oxygen in ether has two bonding pairs (two C-O bonds) and two lone pairs, giving 4 electron domains and sp3 hybridization with a bent geometry.
A. Reducing agent
B. Lewis acid catalyst generating the acylium ion
C. Oxidizing agent
D. Base catalyst
Answer: AlCl3 is a Lewis acid that coordinates with the acyl chloride, generating the electrophilic acylium ion (R-C≡O+) that attacks the aromatic ring.
A. Meta-nitrotoluene
B. Ortho and para-nitrotoluene
C. Para-nitrotoluene only
D. Meta and para-nitrotoluene
Answer: The methyl group is an ortho/para director (activating group) due to hyperconjugation and inductive effects, so nitration gives a mixture of ortho and para products.
A. Zn | Zn2+ || Cu2+ | Cu
B. Cu | Cu2+ || Zn2+ | Zn
C. Zn | Cu || Zn2+ | Cu2+
D. Cu | Zn2+ || Cu2+ | Zn
Answer: In cell notation: anode (oxidation) | anode solution || cathode solution | cathode (reduction). Zn is oxidized (anode) and Cu2+ is reduced (cathode).
A. 2
B. 3
C. 4
D. 5
Answer: DU = (2C + 2 - H)/2 = (12 + 2 - 6)/2 = 4. This corresponds to benzene\'s three double bonds and one ring.
A. Nucleophilic addition to carbonyl
B. Disproportionation of an aldehyde without alpha-hydrogens
C. Radical chain reaction
D. Electrophilic aromatic substitution
Answer: In the Cannizzaro reaction, an aldehyde lacking alpha-hydrogens (like benzaldehyde) undergoes base-induced disproportionation to form an alcohol and a carboxylate salt.
A. Na
B. Mg
C. Al
D. Si
Answer: Mg+ has configuration [Ne]3s1. Removing the second electron from the stable 3s1 is very difficult. Na+ already has a noble gas config [Ne], making its second IE very high too, but Mg2+ removing from [Ne]3s1 to [Ne] is harder than Na+ removing from [Ne] to [He]2s2 2p5.
A. Iodoform (CHI3) and sodium acetate
B. Acetone iodide
C. Isopropanol
D. Acetic acid
Answer: The haloform reaction converts methyl ketones (CH3-CO-) to iodoform (yellow precipitate CHI3) and a carboxylate salt (sodium acetate) using I2 and NaOH.
A. C-C < C=C < C≡C
B. C-C > C=C > C≡C
C. C=C < C-C < C≡C
D. All equal
Answer: Bond dissociation energy increases with bond order: C-C single (~347 kJ/mol) < C=C double (~614 kJ/mol) < C≡C triple (~839 kJ/mol).
A. Gives (E)-stilbene
B. Gives (Z)-stilbene
C. Gives a mixture of E and Z
D. No elimination occurs
Answer: E2 requires anti-periplanar geometry. In the meso compound, the two bromines are anti to each other, and anti-elimination gives (E)-stilbene (trans product).
A. 2-Hydroxypropanoic acid
B. 3-Hydroxypropanoic acid
C. 2-Hydroxyethanoic acid
D. Lactic acid
Answer: The parent chain has 3 carbons with COOH at C1 and OH at C2, giving the IUPAC name 2-hydroxypropanoic acid (lactic acid is the common name).
A. Free radical substitution using Cu(I) salts
B. Nucleophilic aromatic substitution
C. Electrophilic aromatic substitution
D. Addition-elimination
Answer: The Sandmeyer reaction converts aryl diazonium salts to aryl halides (Ar-Cl, Ar-Br, Ar-CN) using copper(I) salts via a free radical mechanism.
A. sp3
B. dsp2
C. sp3d
D. d2sp3
Answer: Ni2+ is d8. With the strong field CN- ligand, all electrons pair up (low spin), and dsp2 hybridization gives a square planar, diamagnetic complex.