The chair configuration and Newman configuration is as below.
1. The given substituted cyclohexane has 1,2 trans configuration. This on conversion to chair form, both Cl and CH3 takes up axial-axial or equatorial-equatorial. But among these two, the latter is stable. This avoids steric hindrance.
². In the newmann projection will be stable in anti staggered form .this is because, it avoids steric strain, torsional strain. Thus, the stable structure is as shown below.
1. Draw the most stable and least stable configurations of the following molecules: a. (Hint: Chair...
6) (10 Pts) Draw the most stable and the least stable Newman projection for the following molecule looking down the indicated bond. Most Stable Least Stable 7) (16 Pts) Draw the most stable and the least stable chair form for the molecule below. You must also draw the Newman projection for both chair conformations looking from the direction indicated by the arrows. More stable chair Newman Projection -more stable chair less stable chair Newman Projection -less stable chair 6) (10...
6) (10 Pts) Draw the most stable and the least stable Newman projection for the following molecule looking down the indicated bond. Most Stable Least Stable 7) (16 Pts) Draw the most stable and the least stable chair form for the molecule below. You must also draw the Newman projection for both chair conformations looking from the direction indicated by the arrows. More stable chair Newman Projection -more stable chair less stable chair Newman Projection -less stable chair
1. Draw the chair conformation for the following molecules: 이 2. Draw the most stable conformation for the following molecules: a) cis-1-ethyl-3-methylcyclohexane b) trans-1-tert-butyl-4-ethylcyclohexane c) (1R,2R,4S) 2,4-dimethyl-1-isopropylcyclohexane
10) a) Draw the most stable and least stable chair conformations of rms- l ethylcyclohexane. b) Caleulate the energy of both structures. 11) Draw the most stable chair conformation of cis-1-ethyl-3-methyleyclohexane.
1. Draw the Neman Projection of the following Promane descriptions Newman projection for most stable Newman projection for least stable conformation conformation 2. Draw the Newman projections for butane looking down the C2-C3 bond through a full 360 degree rotation. Start with the anti-staggered Newman projection then draw and label each Newman projection (staggered, eclipsed, gauche, anti-staggered, fully-eclipsed) for every 60 degrees of rotation Newman projection for most stable Newman projection for second-most stable conformation Conformation Newman projection for least...
1. Draw the MOST stable and the LEAST stable isomer of 3- chloro -4- methylhexane by drawing Newman Projections looking down the bond between Carbon -3 and Carbon-4 2. Circle the most acidic Hydrogen and then explain its acidity as needed with structures and sentençes NH2 OH
Need help with these Orgo Chem problems. mostly with the naming part. thank you Draw the most stable chair conformation of cis-1,2-dimethylcyclohexane 1) Draw the ring flip of the structure in question #1 2) Draw all contributing resonance structures for the following molecules. Make sure to show all arrows showing 3) movement of electrons. :c: Name the following molecules 4) 5) Assign R/S configuration to the molecule, 2-bromobutane, shown Br H H H HyC CH3 2-bromobutane Which of the following...
4. Draw the most stable and most unstable Newman Projection for the following molecules using the rotation around the C3-C4 bond (use the IUPAC rules to number the chain) 5. Draw the two chair conformations for each of the following cyclohexane derivatives and then choose the conformation that is the most stable. Br BA 3 3 3 $ 2879 So ya 6. For the following compounds, identify the chiral carbons with an asterisk (*) and for those that are not...
6. For each of the following molecules, draw the Newman Projection in the most and least stable conformations H xx a CH₃ y. 111111 I I- Br
Draw the most stable isomer by Newman projection and chair structure of the ring.