What are the relative energy levels of the three staggered conformations of 2,3-dimethylbutane when looking down the C2-C3 bond? Ме Me H Me. Me Me Me Me Me Conformation: Me Me H. Me Me A A is the highest energy conformation and C is the lowest (energy level of B is in between the two) B is the highest energy conformation and C is the lowest (energy level of A is in between the two) C is the highest energy conformation and A is the lowest (energy level of B is in between the two) A and B are equal energy, and C is the lowest energy conformation A and B are equal energy, and C is the highest energy conformation

What are the relative energy levels of the three staggered conformations of 2,3-dimethylbutane when looking down the C2-C3 bond? Ме Me H Me. Me Me Me Me Me Conformation: Me Me H. Me Me A A is the highest energy conformation and C is the lowest (energy level of B is in between the two) B is the highest energy conformation and C is the lowest (energy level of A is in between the two) C is the highest energy conformation and A is the lowest (energy level of B is in between the two) A and B are equal energy, and C is the lowest energy conformation A and B are equal energy, and C is the highest energy conformation

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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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.
In the next chapter we'll look at cycloalkanesâ€”saturated cyclic hydrocarbonsâ€”and weâ€™ll see that the molecules generally adopt puckered, nonplanar conformations. Cyclohexane, for instance, has a puckered shape like a lounge chair rather than a flat shape. Why?
Use your answers from Problem 2.48 to complete the table showing correlations between cis,trans and axial,equatorial for disubstituted derivatives of cyclohexane. Draw the alternative chair conformations for the cis and trans isomers of 1,2-dimethylcyclohexane, 1,3-dimethylcyclohexane, 1,4-dimethylcyclohexane. (a) Indicate by a label whether each methyl group is axial or equatorial.
Following is a chair conformation of cyclohexane with the carbon atoms numbered 1 through 6. (a) Draw hydrogen atoms that are above the plane of the ring on carbons 1 and 2 and below the plane of the ring on carbon 4. (b) Which of these hydrogens are equatorial? Which are axial? (c) Draw the alternative chair conformation. Which hydrogens are equatorial? Which are axial? Which are above the plane of the ring? Which are below it?
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.
Fill in the blanks: cis-1,3-Dimethylcyclohexane has two different chair conformations: one withboth methyl groups in __________ positions and one with both methyl groups in ____________ positions.
Following is a planar hexagon representation for one isomer of 1,2,4-trimethylcyclohexane. Draw the alternative chair conformations of this compound and state which of the two is more stable.
Identify the highest and lowest energy conformation. If multiple energy conformations are degenerate, choose only one. Et H. Et Et H. H. MeEt Lowest Energy Me Highest Energy Et H. Et H. Et H. H- H. MeEt Highest Energy Me Lowest Energy Et H. Me H. Me C H H H. Me MeEt Highest Energy Lowest Energy Et H. Me Me H. H H Ме MeEt Lowest Energy Highest Energy OA OB OD
Compare the following conformers of 1-fluoropropan-1-ol. Match each conformer to their corresponding relative energy. Recall, the more stable the conformer the lower the energy. OH CH3 'F 2. HOH 2nd Highest Energy H 2nd Lowest Energy H3C 3. H. ОН Lowest Energy H 'F Highest Energy ČH3 4. H3C, OH 'F 1. >
In the lowest energy conformation of the compound below, how many alkyl substituents are axial? O A. 6 B. 3 O C. 1 O D.O OE. 2
3. Draw both chair conformations for the cyclohexane molecule shown below, and circle the most stable conformation (the methyl group is larger than the hydroxyl group). OH H3C
For the following structural formula, pick the structure that accurately represents its MOST STABLE conformation. CH3 H₂Cl... Br Br Br H₂C O D. O B. O C. O A. CH3 A CH3 B CH3 ... Br 주 Br H3C C CH3 H3C CH3 D