FBISE Class 9th (SSC-l)

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FBISE Class 9th (SSC-l)

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A. Kp = Kc
B. Kp = Kc(RT)^2
C. Kp = Kc(RT)^(-2)
D. Kp = Kc(RT)^4
Answer: Kp = Kc(RT)^(Delta n). Delta n = 2 - (1+3) = -2, so Kp = Kc(RT)^(-2) = Kc/(RT)^2.
A. Tertiary > Secondary > Primary
B. Primary > Secondary > Tertiary
C. Secondary > Primary > Tertiary
D. All equal
Answer: E2 reactivity increases with alkyl substitution because more substituted alkenes (Zaitsev product) are more stable, and tertiary substrates have more beta-hydrogens.
A. mu = sqrt(n(n+2)) BM
B. mu = n(n+2) BM
C. mu = sqrt(n+2) BM
D. mu = 2sqrt(n) BM
Answer: The spin-only formula gives magnetic moment mu = sqrt(n(n+2)) Bohr magnetons, where n is the number of unpaired electrons.
A. Cyclohexanol
B. Adipic acid (hexanedioic acid)
C. Cyclohexanone
D. No reaction
Answer: Hot, concentrated KMnO4 is a strong oxidizing agent that cleaves the C=C double bond in cyclohexene, oxidizing it completely to adipic acid (HOOC-CH2-CH2-CH2-CH2-COOH).
A. Planar (trigonal)
B. Trigonal bipyramidal (pentacoordinate carbon)
C. Tetrahedral
D. Linear
Answer: The SN2 transition state has a pentacoordinate carbon with the nucleophile and leaving group on opposite sides, forming a trigonal bipyramidal arrangement.
A. Principal quantum number (n)
B. Azimuthal quantum number (l)
C. Magnetic quantum number (ml)
D. Spin quantum number (ms)
Answer: The magnetic quantum number (ml) specifies the number of orbitals and their orientation within a subshell, ranging from -l to +l.
A. Ethyl acetate
B. 3-Hydroxybutanal (aldol)
C. Butanal
D. Ethanol
Answer: Two molecules of acetaldehyde undergo aldol condensation: one acts as a nucleophile (enolate) attacking the carbonyl of another, forming 3-hydroxybutanal.
A. Delta G = RT ln K
B. Delta G = -RT ln K
C. Delta G = -RT / ln K
D. Delta G = K / RT
Answer: The fundamental equation is Delta G = Delta G0 + RT ln Q. At equilibrium, Delta G = 0 and Q = K, so Delta G0 = -RT ln K.
A. 1,3-Butadiene
B. 1,4-Pentadiene
C. 1,5-Hexadiene
D. Cyclohexene
Answer: 1,3-Butadiene (CH2=CH-CH=CH2) has alternating double-single-double bonds, creating conjugation where p-orbitals overlap across all four carbons.
A. +0.76 V
B. -0.76 V
C. +0.34 V
D. -0.34 V
Answer: Zn2+/Zn has a standard reduction potential of -0.76 V, meaning zinc is easily oxidized and is a stronger reducing agent than hydrogen.
A. O-H stretch
B. C=O stretch (carbonyl)
C. C-H stretch
D. N-H stretch
Answer: A strong absorption near 1700 cm-1 is characteristic of the C=O stretching vibration, indicating the presence of a carbonyl group (aldehyde, ketone, acid, ester, etc.).
A. Chelating ligands always produce colored complexes
B. Complexes with chelating (multidentate) ligands are more stable than those with equivalent monodentate ligands
C. Chelate rings are always five-membered
D. Chelating ligands are always strong field
Answer: Chelate complexes have greater thermodynamic stability due to favorable entropy changes when multidentate ligands replace multiple monodentate ligands.
A. Rate = k[A][B]
B. Rate = k[A]^2[B]
C. Rate = k[A][B]^2
D. Rate = k[A]^2[B]^2
Answer: The rate law is Rate = k[A]^1[B]^2 for a reaction that is first order in A and second order in B, giving an overall third-order reaction.
A. sp3
B. sp2
C. sp
D. sp3d
Answer: The carbon in a nitrile group has two regions of electron density (one single bond to the adjacent atom and one triple bond to nitrogen), requiring sp hybridization.
A. 22.4 g/mol
B. 44.8 g/mol
C. 89.6 g/mol
D. 11.2 g/mol
Answer: At STP, moles = 0.560/22.4 = 0.025 mol. Molar mass = 2.0/0.025 = 80 g/mol. Wait, let me recalculate: 0.560/22.4 = 0.025, 2.0/0.025 = 80. The answer should be 80 g/mol.
A. Acylbenzene
B. Alkylbenzene
C. Nitrobenzene
D. Di-tert-butylbenzene
Answer: Friedel-Crafts reactions (alkylation and acylation) introduce alkyl or acyl groups. Nitrobenzene formation requires nitration (HNO3/H2SO4), not Friedel-Crafts.
A. 25.3 kJ/mol
B. 50.6 kJ/mol
C. 75.9 kJ/mol
D. 101.2 kJ/mol
Answer: Using Arrhenius: ln(k2/k1) = (Ea/R)(1/T1 - 1/T2). ln(2) = (Ea/8.314)(1/300 - 1/310). Ea = 0.693 x 8.314 x 300 x 310 / 10 = 52,886 J/mol ≈ 50.6 kJ/mol.
A. 3-Oxobutanal
B. 2-Oxobutanal
C. 3-Ketobutanal
D. 1,3-Dioxobutane
Answer: The compound has both aldehyde (CHO, higher priority at C1) and ketone (C=O) groups. Numbering from CHO: C1(CHO)-C2(H2)-C3(=O)-C4(H3), giving 3-oxobutanal.
A. All octahedral complexes are perfectly symmetric
B. Degenerate electronic states cause geometric distortion to remove degeneracy
C. Tetrahedral complexes are always more stable than octahedral
D. Crystal field splitting is always the same for all metals
Answer: The Jahn-Teller theorem states that any non-linear molecule with a degenerate electronic ground state will undergo geometric distortion to remove the degeneracy and lower the energy.
A. 2-Bromopropane (Markovnikov product)
B. 1-Bromopropane (anti-Markovnikov product)
C. 1,2-Dibromopropane
D. No reaction
Answer: Peroxides initiate a free radical mechanism that reverses the normal regioselectivity, adding Br to the less substituted carbon (anti-Markovnikov addition).