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