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- Please don't provide handwritten solution5) relationship between the pairs of structures. NOTE: Each term may be used more than Choose the term from the five terms listed below that BEST describes the once and not all terms need be used. Identical Diastereomers Enantiomers Constitutional isomers Not isomers CH3 CH3 ÇI H3C-Br CH3 Br -CI H,C. D-H H3C- Br H- -D Br CH3 -CI ČH3 OH H3C, CHO OHC, OH OH H. HO CHO OHC CH3 H. OH ÓHPart D. Do the two structures A and B of each pair drawn below represent the same molecule, constitutional isomers, or stereoisomers? If A and B are stereoisomers, further classify them as enantiomers or diastereomers.
- Use flat representation of rings, not chair in the drawing. Determine the most and least stable. Consider the most stable chair for each of these isomers, and then draw the most stable and least stable isomer based on a comparison of the best chair for each one.Give detailed Solution with explanation needed (no need Handwritten answerPlease solve this
- Give detailed Solution with explanation needed..don't give Handwritten answerQuestion 3: Please state whether each of the following molecules is chiral or achiral. If you believe it is achiral, indicate the element of symmetry [plane of symmetry or center of inversion] responsible for the achirality. H3C H3C |H3C OH Br Br -H H CI Br но H Н CI CI CI ОН НН ОН H CI ОН ОН Br- Br H3C. .H неи Н' С2Н5 Н CI CI Br >3. Consider the following compound, which is a derivative of cholesterol. HO Identify all asymmetric carbons and assign their absolute configuration. Write the configuration directly next to each asymmetric carbon in the above image.
- 4. Explain why the protons on the sp³-hybridized carbon of propene (CH3-CH=CH₂) are more acidic than the protons on the sp²-hybridized carbons of propene, even though sp2-hybridized carbons are more electronegative than sp³-hybridized carbons. Use both structures and sentences in your answer.I need an explanation on this problem.2. Assign the stereochemical configuration of the selected carbon-carbon double bonds (E, Z or N (not a stereocenter)) that are indicated by the arrows. a) HN H,, H3CO HO H H