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- Indicate the relationship between each pair. Choose from: configurational stereoisomers,conformers, constitutional isomers, or different formulas (Each term is used at least twice.)cis-1,2-Dimethylcyclohexane is optically inactive even though it has two chirality centers. Explain.The molecule (I) and (II) are || CH3 **H I Identical Enantiomers Diastereomers Constitutional Isomers Next H3C X II
- What term best describes the relationship between the structures below? H, CI H₂N Enantiomers Diastereomers Conformational isomers Constitutional isomers H₂N, HWhat term best describes the relationship between the structures below? Br CI Br Diastereomers Conformational isomers Identical Constitutional isomers Enantiomers CIWhat term best describes the relationship between the structures below? HO CI OH Identical Constitutional isomers Enantiomers Diastereomers Conformational isomers CI
- What term best describes the relationship between the structures below? Constitutional isomers Diastereomers Conformational isomers Identical EnantiomersWhich structure (or structures) represents (or represent) the enantiomer of the molecule below? I OCH 3 &&&* IV I III and IV ||| || OCH3 OH OCH 3 & II || Br III OCH3 H3CO/I IVDetermine the relationship between the isomers of each pair of molecules. Identify whether they are constitutional isomers or conformational isomers or enantiomers or diastereoisomers.
- 2. What term best describes how the following structures/molecules are related to each other? Enantiomers Br b. Diastereomers c. Identical d. Constitutional Isomers سال Br Br Br91/ Draw examples of the following: a ) Ameso, Enantiomers and diastereomers compounds with the formula CaH18. b) Acompound with tow chirality centers (S, R) and (R, R). らにDraw all configurational isomers of C4H11N that are optically active.