2) Draw a hexane chain that has 2 carbon substituents and 1 halogen. Translate this drawing to themost stable Newman projection.

We need a six carbon chain out of which 2 carbon substituent and one halogen. I take 4- chloro-2,3-…

Answered: 2) Draw a hexane chain that has 2…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 4E: Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This...

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Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed down the red bond in the direction of the red arrow. Your projection should be oriented as shown by the arrow marked up. So the CH2SH group on the front carbon should be above the H and H3C groups, no matter which template you use
how to draw a trans-1,3-dimethylcyclohexane and its ring flip. (please also draw out each hydrogen!!!)
Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed down the red bond.
Draw the most stable Newman projection for the following alkanes looking down the C-C bond pointed to by the arrows.
Look at a cyclohexane model:a. Mark the axial bonds. Hold carbon atoms 1, 2, 3, 4, 5, and 6 firmly and flip up carbon 4. What is the resulting conformation? b. Then holding carbons 2, 3, 4, 5, and 6 firmly, flip down carbon What is now the resulting conformation?
Draw the potential energy of the molecule circled at the top. Draw the other 3 Newman projections based on the one already drawn by rotating the back carbon clockwise. Explain your answers
Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.
Label each ring in Figure 7.2 cis or trans.
Using your model of butane (CH3CH2CH2CH3) , complete the following graph of the anglebetween the two Me groups vs. potential energy. a. Label each Newman projection of butane on the graph with the words staggered, eclipsed, gauche, and anti, as appropriate. (Note that some structures will have more than one label.) b. Draw a wedge and dash bond representation of butane in its lowest P.E. conformation.
Identify circle the alkanelike portions of the following molecules: a. b. c. d.
Please draw using skeletal structure and draw substituents as far to the left, according to the priorities listed (1-5) in second picture
Draw a hexane chain that has 2 carbon substituents and 1 halogen. Translate this drawing to the most stable Newman projection.

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2) Draw a hexane chain that has 2 carbon substituents and 1 halogen. Translate this drawing to the most stable Newman projection.