Which Newman projection correctly identifies the HIGHEST energy conformation of the below molecule? Br. CH3 H9C5...
Which Newman projection correctly identifies the HIGHEST energy conformation of the below molecule? Br CH3 • H9C5 Br -Н НХ Х H3C H3CBr НА H9C5 o H3C Br -С5Нэ Н Н H9CsBr -СН3 HTS
Which is the most stable Newman projection of the molecule below, assuming a Br-CH3 gauche interaction is 0.5 kcal/mol and a CH3-CH3 gauche interaction is 1.0 kcal/mol? Br CH3 - CH- -CH 2 -CH3 CH3 CH3 CH3 H Н. Br Br H H H Br H H H CH3 Br сн. сн., H a. сн. c. H d. CH Oooooooo Moving to another question will save this response MacBook AS ese
In-Class Worksheet In the box below each molecule, draw Newman projections for the structures A, B, and C shown from the perspective indicated. For each Newman projection that you've drawn, indicate if there are any eclipsed bonds or 1. gauche butane interactions. H H CH3 H3C CH3 CH3 H. H3C CH3 H CH3 H H Structure C Structure B Structure A Structure A can exist in a lower energy conformation by undergoing a bond rotation; draw the Newman projection of...
Given the following perspective drawing: H3C "CH CH3 Choose the Newman projection, from the choices below, that is identical in constitution, configuration and conformation br X CH2CH3 H H3CH2C CH2CH3 Bry CH₃ BrQCH2CH3 F2CH3 O
Conformations of Alkanes and Cycloalkanes 1) Draw a Newman projection of the anni conformation of 1.2-dichloroethane che conformation of 1.2-dichloroethane 2) Draw a Newman projection of the 5) Sight along the C2-C3 bond of 2-methylbutane and draw each of the staggered conformations 4) Arrange the following conformations from lowest to highest energy. CH CH 5) Circle the Most stable conformation of the molecule shown below. н сн, YI 6) Circle the Most stable conformation of the molecule shown below.
Which Newman projection represents the most stable conformation of (CH),CHCH(CH)2? CH3 CH3 СCH3 (B) (A) CH3 H CH3 "СHз CHз CH3 CH3 н CH3 (D) (C) H. tCH3 CH3 CH3 Н Н CH3 CH3
1. Use the following structure to draw Newman Projections (each subsequent projection with the back carbon rotated 60" clockwise), Label the projection that is highest in energy and lowest in energy. Explicitly label all H's and CHY's. The arrow denotes the "front" carbon. Use this position to start your first Newman Projection Hae H | 改改改改 2. Finish each Newman Projection to correctly represent the following molecule in the box. OH Br CH3 0月
check and solve the empty ones please
Which of the following is a Newman projection for the following compound as viewed down the indicated bond? сун 9. Draw the most stable conformer of the following compound. C/ 10. Draw the Newman projection for the highest energy and lowest energy conformation of the following compound. (size: Br > CH) Br me ) be ved me TH me heighest 11. Which of the following molecule is trans-1,2-dimethylcyclohexane? A) B) D) Othe 12....
2. Look at the moleculebelow. Together in your group, draw a Newman projection in the highest possible energy this molecule can exist. Look directly at carbon 1, and have carbon 2 in the back. CH3 Br CH3
Br Choose the Newman projection, from the choices below, that is identical in constitution, configuration and conformation Given the following perspective drawing: CH.CH E 3 HC F Choose the Newman projection, from the choices below, that is identical in constitution, configuration and conformation CH3 CH2CH3 F CH2CH3 CHE CH2CHE CH₂CH₂ Submit Answer Tries 0/1