FBISE Class 9th (SSC-l)

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FBISE Class 9th (SSC-l)

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A. They must be gauche
B. They must be anti-periplanar (180 degrees dihedral angle)
C. They must be syn-periplanar (0 degrees dihedral angle)
D. There is no geometric requirement
Answer: E2 requires an anti-periplanar arrangement where the C-H and C-LG bonds are at 180 degrees, allowing maximum orbital overlap for the developing pi bond.
A. Maximum
B. Equal to E0
C. Zero
D. Negative
Answer: At equilibrium, Q = K and Delta G = 0, so from Delta G = -nFE, we get E = 0. The cell has no driving force at equilibrium.
A. NMR spectroscopy
B. UV-Vis spectroscopy
C. IR spectroscopy
D. Mass spectrometry
Answer: IR spectroscopy measures the absorption of infrared radiation by molecular vibrations (stretching and bending of bonds), revealing functional groups and molecular framework.
A. Number of equivalent protons
B. The electronic environment of the proton
C. The number of neighboring protons
D. The molecular weight
Answer: Chemical shift reflects the shielding/deshielding of a proton by surrounding electrons. Deshielded protons (near electronegative atoms) appear at higher delta values.
A. First order
B. Second order
C. Third order
D. Zero order
Answer: E1 is unimolecular: only the substrate is involved in the rate-determining step (carbocation formation), so Rate = k[substrate], making it first order.
A. Rate constant decreases exponentially
B. Rate constant increases exponentially
C. Rate constant remains the same
D. Rate constant increases linearly
Answer: As T increases, Ea/RT decreases, making e^(-Ea/RT) larger, so k increases exponentially with temperature.
A. Enthalpy when 1 mole burns in excess oxygen at standard conditions
B. Enthalpy when all moles burn completely
C. Enthalpy of formation of combustion products
D. Enthalpy per gram of fuel burned
Answer: Standard enthalpy of combustion is the enthalpy change when 1 mole of a substance undergoes complete combustion in excess O2 under standard conditions (298 K, 1 atm).
A. Polyethylene
B. Polypropylene
C. Polytetrafluoroethylene (PTFE/Teflon)
D. PVC
Answer: Tetrafluoroethylene (CF2=CF2) undergoes addition polymerization to form PTFE (Teflon), where the double bond opens to form long chains.
A. All electrons are paired
B. Zero pairing energy because all t2g and eg orbitals are singly occupied
C. Maximum splitting
D. Delta_o equals the pairing energy
Answer: In high-spin d5, each of the five d-orbitals gets one electron (t2g3 eg2) with no pairing, so no pairing energy is required.
A. Nucleophilic attack on the carbocation
B. Loss of the leaving group to form the carbocation
C. Deprotonation
D. Formation of the transition state
Answer: The slowest step in SN1 is ionization: the departure of the leaving group to form a carbocation intermediate. This step has the highest activation energy.
A. t1/2 = 0.693/k
B. t1/2 = [A]0/2k
C. t1/2 = 1/(k[A]0)
D. t1/2 = 2.303/k
Answer: For first-order reactions, t1/2 = ln(2)/k = 0.693/k, which is independent of the initial concentration.
A. 3-Bromo-1-butene
B. 2-Bromo-3-butene
C. 1-Bromo-2-butene
D. 3-Bromo-2-butene
Answer: Numbering gives the double bond the lowest locant: C1=C2-C3(Br)-C4. Bromine is on C3, so the name is 3-bromobut-1-ene.
A. n -> pi*
B. pi -> pi*
C. sigma -> sigma*
D. n -> sigma*
Answer: Sigma bonds are the strongest, so sigma -> sigma* transitions require the highest energy (shortest wavelength), typically in the far UV region.
A. Less than 7
B. Equal to 7
C. Greater than 7
D. Depends on the indicator
Answer: The salt formed (e.g., NaCl) is neutral, so the pH at equivalence is exactly 7 for strong acid-strong base titrations.
A. A ligand that forms one bond to the metal
B. A ligand that forms two bonds to the metal
C. A ligand that forms six bonds to the metal
D. A ligand that carries a -2 charge
Answer: A bidentate ligand has two donor atoms that simultaneously coordinate to the metal center, forming a chelate ring (e.g., ethylenediamine, oxalate).
A. lambda = h/mv
B. lambda = h x mv
C. lambda = mv/h
D. lambda = h/2mv
Answer: The De Broglie equation states lambda = h/p = h/(mv), where h is Planck\'s constant, m is mass, and v is velocity, predicting wave-particle duality.
A. Bromination of benzene
B. Addition of HBr to propene
C. Chlorination of methane
D. Hydrolysis of an ester
Answer: HBr adds across the C=C double bond in propene. The electrophilic H+ attacks the pi bond first, followed by nucleophilic Br- attack.
A. m = (M x I x t) / (n x F)
B. m = (n x F) / (M x I x t)
C. m = (M x F) / (n x I x t)
D. m = (I x t) / (M x n x F)
Answer: Faraday\'s first law: mass deposited (m) = (M x I x t)/(n x F), where M is molar mass, I is current, t is time, n is electrons transferred, and F = 96485 C/mol.
A. IR spectroscopy only
B. 1H NMR spectroscopy
C. UV-Vis spectroscopy
D. Flame test
Answer: 1H NMR gives different splitting patterns: 1-propanol shows a triplet for the CH3, while 2-propanol shows a distinctive septet for the CH and a doublet for two equivalent CH3 groups.
A. Unimolecular
B. Bimolecular
C. Termolecular
D. Quadrimolecular
Answer: Molecularity is the number of molecules that come together in an elementary step. Three simultaneous collisions give termolecular (trimolecular) molecularity.