Chiral withTry to manipulate the cis and trans isomers of 1-iodo-1-propene by rotating bonds but without breaking bonds. The two structures are nonsuperimposable mirror images, achiral compounds that differ only in atom orientation in space.2. Starting with cis-1-iodo-1-propene, add two bromine atoms across the double bond at C1 and C2 such that both atoms are added to the top of the bond; then create the mirror image of this structure. The two compounds are diastereomers (stereoisomers that are

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