Draw the skeletal structure of (S)-3-bromo-3- iodohexane. Use a dash or wedge bond to indicate the relative relationship of substituents, where applicable. Drawing
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- (a) What is the IUPAC name for the following molecule (including absolute configurations if required)? (b) Draw the Newman projections looking down the C3-C4 bond that represent all the three staggered conformations for the molecule shown above. (c) Given that the strain energies below, calculate the strain energies for each conformer and identify which is the most stable. Gauche interaction Strain Energy HOCH3 0.0 kJ mol- HOCH;CH; |0.4 kJ mol- 3.8 kJ mol- | 4.3 kJ mol- CH;CH3 CH;CH2CH3 |CH2CH; CH2CH; 4.6 kJ mol- Newman Projection of Conformer 1 Strain Energy of Conformer 1 Newman Projection of Conformer 2 Strain Energy of Conformer 2 Newman Projection of Conformer 3 Strain Energy of Conformer 3Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the cyano with the ortho position in benzonitrile. CEN benzonitrile • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.Draw Newman projections for the anti, eclipsed, gauche and fully eclipsed conformations of Butane. Indicate their relative stabilities and the reasons for your ranking-need to discuss the stresses involved in each case. Using suitable specific conformers of specific structures as examples, explain the difference between (a) angle strain (b) torsional strain and (c) steric strain. Need to draw the confomers and structures 4) Draw the most stable conformers using chair structures of the following: (c) cis-1,2-Dibromocyclohexane (d) trans-1,2-Dibromocyclohexane (e) cis-Decalin (f) trans-Decalin . Draw the most stable conformers of trans-1-Bromo-4-methylcyclohexane and cis-1-Bromo-4-methylcyclohexane. Which is more stable? Explain the reason for your answer. Need to include a discussion of 1,3-Diaxial interaction
- Please don't provide handwritten solution .....Quiz: Exam 3 (Final) -> A ilearn.laccd.edu/courses/132371/quizzes/939964/take/questions/2012.. Fill in the blanks: The name for is Cl The name for is The common name for is H,C HO The common name for is Br The name for isWhat is the systematic name for the molecule depicted by the following bond line structure? Decide what the longest C-C chain is (parent) and then decide which substituents are there and how to number it to give the lowest locants. Make sure each substituent gets a locant. Separate letters from numbers by a dash, and numbers from each other by a comma. Do not put any spaces in your name.
- I had entered the answer without the cis- which was wrong but I just want to be sure if the name is correct, thank youGive detailed Solution with explanation needed withs tructures. Don't give Handwritten answer...Jeet huoy fimdua uoy ner Question 2 For the cis-1,3-dibromocyclhexane, draw its planar structure with wedge and dash notations. Then, draw its diastereomers in planar structures with wedge and dash notations.

