Question

Calculate the percentage of the most stable conformer of cis-4-tert-butylcyclohexan-1-ol at 25C

Calculate the percentage of the most stable conformer of cis-4-tert-butylcyclohexan-1-ol at 25C

Homework Answers

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
give the chair conformation for the most stable configuration of: Trans-1-methyl-3-isopropylcyclohane Cis-1-tert-butyl-2-methylcyclohexane
give the chair conformation for the most stable configuration of: Trans-1-methyl-3-isopropylcyclohane Cis-1-tert-butyl-2-methylcyclohexane
tert-Butyl groups "lock" cyclohexanes into a conformation where the tert-butyl group occupies an equatorial position and...
tert-Butyl groups "lock" cyclohexanes into a conformation where the tert-butyl group occupies an equatorial position and the ring-flip equilibrium is essentially stopped. To verify this fact, write the ring-flip equilibrium of trans-1-tert-butyl-4-methylcyclohexane such that the least stable chair conformation is the product (this will cause the ΔE to be greater than (or equal to) zero. T = 298 K R = 8.315 J/mole-K H - Substituent Interaction 1,3-Diaxial Strain (kJ/mole) H ←→ CH3 3.8 H ←→ C(CH3)3 11.4 ΔE -...
One can calculate the relative amounts of cis and trans 4-tert-butylcyclohexanols in your synthetic mixture by...
One can calculate the relative amounts of cis and trans 4-tert-butylcyclohexanols in your synthetic mixture by looking at the signals in the NMR due to the proton attached to the carbon bearing the OH group. They have different chemical shifts because; Group of answer choices they are in different magnetic environments. because one is primary and the other is secondary.. because on is cis to the tert-butyl group and the other is trans. none of the above. 2) Deutero-chloroform is...
Draw the most and least stable chair conformations for cis-1-ethyl-4-propylcyclohexane. Explain in 2-3 complete sentences why...
Draw the most and least stable chair conformations for cis-1-ethyl-4-propylcyclohexane. Explain in 2-3 complete sentences why you assigned your conformations as most and least stable.
1A.The ___ conformer of an alkane chain and the ____ of cyclohexane are the most stable....
1A.The ___ conformer of an alkane chain and the ____ of cyclohexane are the most stable. eclipsed/boat eclipsed/chair staggered/boat staggered/chair 1B.All of the carbons in cyclohexane are on the same plane. true false and the H's too 1C. The chair conformer of cyclohexane is ____ stable than the boat conformer because the axial H’s on C-1 and C-4 are _____ each other. more/nearest more/farthest less/nearest less/farthest 1D.Strain between the ______ H’s on C-1 and C-4 in cyclohexane is due to...
a) Calculate BE/A (in MeV) for 12C. Stable and relatively tightly bound, this nuclide is most...
a) Calculate BE/A (in MeV) for 12C. Stable and relatively tightly bound, this nuclide is most of natural carbon. (Assume 1 u = 931.5 MeV/c2. Give your answer to at least 2 decimal places.) Incorrect: Your answer is incorrect. MeV (b) Calculate BE/A (in MeV) for 11C. Incorrect: Your answer is incorrect. MeV Is the difference in BE/A between 12C and 11C significant? One is stable and common, and the other is unstable and rare. (Assume the difference to be...
The LEAST stable conformational isomer of cis-1-isopropyl-2-methylcyclohexane will have: A. Both isopropyl and methyl groups in...
The LEAST stable conformational isomer of cis-1-isopropyl-2-methylcyclohexane will have: A. Both isopropyl and methyl groups in axial positions B. Both isopropyl and methyl groups in equatorial positions C. The isopropyl group in an axial position and the methyl in an equatorial position D. The isopropyl group in an equatorial position and the methyl in an axial position E. None of the above Please show work/provide reasoning. Thanks!
1) Use the integrated rate law to calculate the concentration of tert-butyl chloride at t =...
1) Use the integrated rate law to calculate the concentration of tert-butyl chloride at t = ( 1.5) X (half life) if half life is 23.5 seconds 2) Explain why the rate can't be determined simply examining the balanced equation? 3) propose an experiment to determine the activation energy of this reaction
The enthalpy of combustion (ΔH°c) of cis-1-ethyl-4-methylcyclohexane (C9H18) is -5875.10 kJ/mol. Using the appropriate information given...
The enthalpy of combustion (ΔH°c) of cis-1-ethyl-4-methylcyclohexane (C9H18) is -5875.10 kJ/mol. Using the appropriate information given below, calculate the enthalpy of formation (ΔH°f), in kJ/mol, for cis-1-ethyl-4-methylcyclohexane. Report your answer to two decimal places. ΔH°f (CO2 (g)) = -393.51 kJ/mol ΔH°f (H2O (l)) = -285.83 kJ/mol
Route A: 1-chloropropane +Mg -------Et2O----> propylmagnesium chloride --------i.Et2O ii.H2O----> 2-methylheptan-4-ol ----------NaOCl---------> 2-methylheptan-4-one Route B: 1-chloro-2-methylpropane +Mg...
Route A: 1-chloropropane +Mg -------Et2O----> propylmagnesium chloride --------i.Et2O ii.H2O----> 2-methylheptan-4-ol ----------NaOCl---------> 2-methylheptan-4-one Route B: 1-chloro-2-methylpropane +Mg ---------Et2O-----> isobutylmagnesium chloride ---------i.Et2O ii.H2O----> 2-methylheptan-4-ol ----------NaOCl---------> 2-methylheptan-4-one Assume both approach were similar yielding: what would make one approach superior over the other if this experiment was being done in a small lab on the ~5g scale? What about if you had to do this reaction on the 100kg scale in a pilot chemical plant?
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT