which conformation is more stable and has a lower energy ? Howie - BICHZECHz - which...

Question

Question

which conformation is more stable and has a lower energy ?
Howie - BICHZECHz - which conformation is more stable and has a lower energy?

science chemistry

Answer 1

Answer #1

aky group always prefer to be at equiterial Solution :- belky proces always prefer to et al position. (e=equitorial, a= axial

Answer 2

Similar Homework Help Questions

Which comformation is the more stable , and has a lower energy ? Hw Dre Thursday...

Which comformation is the more stable , and has a lower energy ? Hw Dre Thursday lyspia Ctyfets A has alowwer Canlormat1ao is oae slable feण Which CHCHE A. conformaon s morestable i
which are more stable? CH3 Cite CH3 CH Conformation 2 for isomer A (A2) Conformation 1 for isomer A (A1) Question 3:...

which are more stable? CH3 Cite CH3 CH Conformation 2 for isomer A (A2) Conformation 1 for isomer A (A1) Question 3: Which conformation is more stable for isomer A? Why? 3. Draw two different chair conformations for model isomer B CAB CH3 CAB Chs Conformation 2 for isomer B (B2) Conformation 1 for isomer B (B1) Question 4: Which conformation is more stable for isomer B? Why?
Draw one chair conformation of cis-2-methylcyclohexanol and one chair conformation of trans-2-methylcyclohexanol. Which is more stable?

Draw one chair conformation of cis-2-methylcyclohexanol and one chair conformation of trans-2-methylcyclohexanol. Which is more stable?

6) The twisted boat conformation of cyclohexane is actually a slightly lower energy conformation than the...

6) The twisted boat conformation of cyclohexane is actually a slightly lower energy conformation than the boat conformation. Which of the following accurately describes one factor involved in this structural behavior? A) lower angle strain in the boat B) higher torsional strain in the twisted boat C) fewer unfavorable steric factors in the twisted boat D) increased rotational freedom in the boat E) lower bond strain in the boat
Ethylene glycol (CH2OHCH2OH) is unusual in that the gauche conformation is more stable than the anti...

Ethylene glycol (CH2OHCH2OH) is unusual in that the gauche conformation is more stable than the anti conformation. Offer an explanation. Be sure to answer all parts. The conformation , making it the stable conformation.
2 factors that are responsible for raising the energy of the less stable conformation

2 factors that are responsible for raising the energy of the less stable conformation

1. Draw the most stable (lowest energy) chair conformation of the following molecule (5 points) 2....

1. Draw the most stable (lowest energy) chair conformation of the following molecule (5 points) 2. Draw the least stable (highest energy) chair conformation of the following molecule (5 points)
Which of the following Newman projections that represent the most stable conformation of 2,3-dimethylbutane. Which of...

Which of the following Newman projections that represent the most stable conformation of 2,3-dimethylbutane. Which of the following Newman projections that represent the most stable conformation of 2,3-dimethylbutane.
Which of the following two conformations of cis-1-isopropyl-4-methylcyclohexane is more stable? Use the strain energy increments...

Which of the following two conformations of cis-1-isopropyl-4-methylcyclohexane is more stable? Use the strain energy increments in the table below estimate the energy difference (a positive number) between them. Which of the following two conformations of cis-1-isopropyl-4-methylcyclohexane is more stable? Use the strain energy increments in the table below estimate the energy difference (a positive number) between them. 1,3-Diaxial Strain Energies for Monosubstituted Cyclohexanes SubstituentkJ/mol Substituent kJ/mol 0.4 0.5 -C CH, ethynyl 0.85 2.95 2.95 -CH-CH23.55 3.64 -CH2CH 3.65 -CN,...

Help with organic chemistry.Answer all of the questions please. Which is the most stable conformation? Are...

Help with organic chemistry.Answer all of the questions please. Which is the most stable conformation? Are the results for 1, 3- and 1.4- isomers similar to those for the 1, 2-isomers? Does the ring location of the two methyl substituents influence the relative energy differences?