A) dsp2 B) sp C) sp2 D) sp3
A) Four B) Three C) Five D) Two
A) Only for carbon B) Only for nitrogen C) No D) Yes
A) Chiral carbon B) Chiral sulfur C) Chiral nitrogen D) Chiral metal
A) The hybridization changes B) A meso compound is formed C) An enantiomer is produced D) The molecule becomes achiral
A) Racemization B) Oxidation C) Reduction D) Stabilization
A) Primary amine B) Neutral ammonia C) Quaternary ammonium D) Secondary amine
A) Three B) Four C) One D) Two
A) Trigonal bipyramidal B) Planar C) Tetrahedral D) Linear
A) Only when sp3 B) No C) Only when sp2 D) Yes
A) trans-isomer B) fac-isomer C) cis-isomer D) mer-isomer
A) Λ and Δ B) D and L C) E and Z D) R and S
A) They are racemic mixtures B) They are meso compounds C) They contain only sp2 centers D) The atoms are not hybridized
A) A hydrogen atom B) A covalent bond C) The electron pair D) A metal ion
A) d-orbital only B) sp3 C) sp2 D) f-orbital only
A) Stereogenic center B) Chiral center C) Symmetry center D) Configuration center
A) 2n B) 2+n C) n2 D) n/2
A) Only triple bonds B) Only double bonds C) Single or double bonds D) Only single bonds
A) Lowest atomic number B) Highest atomic number C) Counter-clockwise direction of priority D) Clockwise direction of priority
A) Meso compounds B) Non-superposable mirror images C) Superposable mirror images D) Identical molecules
A) Compounds with no stereocenters B) Non-superposable, non-identical, non-mirror image molecules C) Superposable mirror images D) Non-superposable mirror images
A) The number of substituents B) The arrangement of atoms around the center C) The bond length D) The chemical composition |