Photochemical chlorination of 1,2-dibromoethane gives a mixture of two stereoisomers of C2H3Br2Cl. Write their structural formul
as. Are they enantiomers or diastereomers? Are they chiral or achiral? Are they formed in equal amounts?
1 answer:
Answer:
Enantiomers
Chiral
Yes they will be formed in equal amount.
Explanation:
The Two possible stereo isomers are formed due to generation a chiral center in the molecule.
There will be a carbon with all the four groups different.
The two isomers will be called as enantiomers, which are non super-imposable mirror image of each other.
They are named as "R" or "S'" based on the selection rule.
The IUPAC names are also given in the figure.
The two isomers will be formed in equal amount as during photochemical chloriantion of a compound free radicals are generated (which are trigonal planar) and the other radical may attack from either side (front side or back side) giving the two stereo-isomers.
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Answer:
sp3 - 1,2,13,16,18,19
sp2- 3,4,5,6,7,8,9,10,11,12,14,15,17
sp- 0
Explanation:
Hybridization is the idea that atomic orbitals fuse to form newly hybridized orbitals, which in turn, influences molecular geometry and bonding properties (Chemlibretexts).
Carbon atoms that are singly bonded are sp3 hybridized, carbon atoms that are doubly bonded are sp2 hybridized while carbon atoms that are triply bonded are sp hybridized.
Sp3 hybridized atoms have a tetrahedral geometry, sp2 hybridized atoms have a trigonal planar geometry while an sp hybridized atom has a linear geometry.
The hybridization state of each atom in the compound has been shown in the answer section.
