Photochemical chlorination of 1,2−dibromoethane gives a mixture of two stereoisomers of c2h3br2cl. draw the structure of one of the products

See the structure at the bottom-left corner of the sketch attached.

Replacing an H atom with a Cl atom in a 1,2-dibromoethane molecule produces a molecule of C₂H₃Br₂Cl. Its structural formula is show in the top-left corner of the sketch attached.

The molecule contains no double or triple bonds. It has no E/Z isomers. The two stereoisomers can only be enantiomers. A red asterisk * is placed next to the only chiral carbon in this molecule.

That carbon atom is connected to

The two isomers are mirror images about this carbon atom. Indicate how the four groups are arranged in space using the wedge and dash notation.

The last row of this sketch shows the structure of both isomers. The question is asking for only one. Showing either of them should work.

d.) circle motion requires a force to give it a centripetal acceleration.

the product of the pressure and volume is also constant