Indicate whether the pair of structures shown represent stereoisomers, constitutional isomers, different conformations of the same compound, or the same conformation of a compound viewed from a different perspective. Note that cis, trans isomers are an example of stereoisomers. Br H₂C NH₂ -Br Br -Br CH3 -NH₂2 1

Draw a pair of cis/trans stereoisomers with a molecular formula of C7H14.  Label the cis compound and the trans compound.

HN- H3C HN -NH "CH3 OH H. CH3 H,C. Br H3C CH3 CH3 HO. Br HO,

We have learned that isomers (molecules with the same molecular formula) can have different relationships, and these relationships can be made more clear by comparing IUPAC names. Constitutional isomers will differ in the main part of the name. Stereoisomers will differ only in the stereochemical prefix part of the name (cis/trans). Conformational isomers will actually have the same name, but different energies. Two structures that have the same names and the same energies are identical. What is the relationship between these two structures? ********ITS NOT IDENTICAL ****** that’s what I put and it was wrong……

We have learned that isomers (molecules with the same molecular formula) can have different relationships, and these relationships can be made more clear by comparing IUPAC names. Constitutional isomers will differ in the main part of the name. Stereoisomers will differ only in the stereochemical prefix part of the name (cis/trans). Conformational isomers will actually have the same name, but different energies. Two structures that have the same names and the same energies are identical. What is the relationship between these two structures?

Indicate whether the pair of structures shown represent stereoisomers, constitutional isomers, different conformations of the same compound, or the same conformation of a compound viewed from a different perspective. Note that cis, trans isomers are an example of stereoisomers. H3C. H3C. -CH3 ČH3 Br Br H. Br Br 9 more group attempts remaining Submit Answer Retry Entire Group > >

Is there a difference in the stability of the two cyclohexane conformations?

Classify the pair of compounds as the same compound, enantiomers, diastereomers, constitutional isomers, or not isomeric. Also, select the correct IUPAC name, including the correct (R) or (S) designation, for each. H Br Br CH3 H H3C Br H Br Br Br Compound 1 Compound 2 The compounds are identical diastereomers not isomeric constitutional isomers enantiomers The correct IUPAC names are: Compound 1: (2R,3R)-1,2,3-tribromobutane, Compound 2: (2R,3R)-1,2,3-tribromobutane Compound 1: (2R,3S)-1,2,3-tribromobutane, Compound 2: (2S,3S)-1,2,3-tribromobutane Compound 1: (2S,35)-1,2,3-tribromobutane, Compound 2: (2R,3S)-1,2,3-tribromobutane Compound 1: (2R,3R)-1,2,3-tribromobutane, Compound 2: (2S,3R)-1,2,3-tribromobutane

Please don't provide handwriting solution

Indicate whether the pair of structures shown represent stereoisomers, constitutional isomers, different conformations of the same compound, or the same conformation of a compound viewed from a different perspective. Note that cis, trans isomers are an example of stereoisomers. CH₂CH3 -CH₂CH3 H₂N. CH₂CH3 -NH₂ CH₂CH3 H₂N- NH₂