3.(a)i.ii.a)HCH3HH3CCH3CH₂CH₂CH3HCH3Convert each of the above Newman projections into a solid/dashed wedge representation ofthe specific conformer. Use the given template where the front and back carbons must beconverted as marked. One hydrogen atom has been drawn as a reference. Make sure youput a hydrogen atom or alkyl group at the end of each of the remaining bonds in the template.Hb) HoH3C(b)back carbon-HН."XXCH3CH₂CH3front carbon(c)H3Cc)HCH₂CH3Н' HCH3H.ŅConvert each Newman projection to a line structure similar to the one shown in #2. Draw thelongest straight chain of carbon atoms in a 'zigzag' form horizontally. You do not need to showsolid/dashed wedges for the substituents on the parent chain.(a) Line structure(b) Line structure(c) Line structure

The convert a Newman projection to solid/dashed wedge, first we have to check the substituents that…

3. (a) i. a) ii. CH3 H. CH3 H H3C b) (b) H H. H3C back carbon- H CH₂CH₂CH3 H CH3 Convert each of the above Newman projections into a solid/dashed wedge representation of the specific conformer. Use the given template where the front and back carbons must be converted as marked. One hydrogen atom has been drawn as a reference. Make sure you put a hydrogen atom or alkyl group at the end of each of the remaining bonds in the template. CH3 CH₂CH3 H. XX front carbon c) (c) H H3C CH₂CH3 HPH CH3 H XX Convert each Newman projection to a line structure similar to the one shown in #2. Draw the longest straight chain of carbon atoms in a 'zigzag' form horizontally. You do not need to show solid/dashed wedges for the substituents on the parent chain. (a) Line structure (b) Line structure (c) Line structure

3. (a) i. a) ii. CH3 H. CH3 H H3C b) (b) H H. H3C back carbon- H CH₂CH₂CH3 H CH3 Convert each of the above Newman projections into a solid/dashed wedge representation of the specific conformer. Use the given template where the front and back carbons must be converted as marked. One hydrogen atom has been drawn as a reference. Make sure you put a hydrogen atom or alkyl group at the end of each of the remaining bonds in the template. CH3 CH₂CH3 H. XX front carbon c) (c) H H3C CH₂CH3 HPH CH3 H XX Convert each Newman projection to a line structure similar to the one shown in #2. Draw the longest straight chain of carbon atoms in a 'zigzag' form horizontally. You do not need to show solid/dashed wedges for the substituents on the parent chain. (a) Line structure (b) Line structure (c) Line structure

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter7: Cycloalkanes

Section: Chapter Questions

Problem 17E: Build a model of methylcyclohexane, and use the model to complete the following Newmanprojections of...

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Between the cis and trans configuration of 1-chloro-3-methylcyclohexane, which is the most stable stereoisomer and configuration? To prove your argument, use your models or a modelling software to model cis- and trans-1-chloro-3-methylcyclohexane (show all the hydrogens and ensure proper chair conformation) and use arrows to show where steric strain occurs. Include these photos in your answer.
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