Answered: Draw the two chair conformations of…

Draw the two chair conformations of each compound, and label the substituents as axial and equatorial of trans-1-ethyl-2-isopropylcyclohexane

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter2: Alkanes And Cycloalkanes

Section: Chapter Questions

Problem 2.35P: Consider 1-bromo-2-methylpropane and draw the following. (a) The staggered conformation(s) of lowest...

See similar textbooks

Related questions

Q: Draw the two chair conformations of cis-1-tert-butyl-2-ethylcyclohexane, which one is most stable.

Q: Consider 1-bromo-2-methylpropane and draw the following. Q) The staggered conformation(s) of highest…

A: The structure of 1-bromo-2-methylpropane is shown below: The conformations of alkanes are isomers…

Q: Is this a chair conformation of cis-1,3-dimethylcyclohexane or of trans-1,3-dimethylcyclohexane?

A: Chemical compounds having same molecular formula and different spatial arrangement of atoms or group…

Q: H "CO2H a.) Group a is Group b is Group c is, H CH3 b.) Group a is Group b is Group c is c.) Group a…

Q: the energy diagram corresponding to each conformer by writing the confomers (and Newman projection…

A: Higher the 1,3-diaxial interactions more would be the unstability of the conformation.

Q: draw chair conformation for trans-1-isopopyl-3-methylcyclohexane

A: The chair conformation for trans-1-isopopyl-3-methylcyclohexane are shown as,

Q: H C-Ć- C -CI H Following is the structural formula of 1,2– dichloroethane. H a) Draw Newman…

A: Newman projections of 1,2 dichloroethane is represented in below.

Q: Which conformation is the most STABLE STAGGERED conformation of 2,3-dimethylbutane along the C2-C3…

A: The stability of any compound is determined by the energy it possess. The less is the energy of the…

Q: cyclonexane. föllowing dicate which of the two conformations is the most stable. ОН Fl. CH3 Cl

A: Given : We have to write the most stable structure.

Q: 7. Which one of the following conformations of disubstituted cyclohexanes is expected to be the most…

A: Presence of one bulky methyl group at axial position will cause two gauche butane interaction. This…

Q: The most stable conformer of trans-1-isopropyl-3- methylcyclohexane?

A: Conformers are the isomers which are differ bysingle bond rotation in the molecule.The given…

Q: Consider the isomers of tert-butylcyclohexanol in conformational structures. Two are…

Q: Why is this chair conformation the most stable trans-1-chloro-3-flurocyclohexane? Wouldn't the…

A: This question is related to stability of conformations

Q: Based on naming branched alkyl substituents, and draw all possible alkyl groups having the formula…

A: Different organic compounds can have different molecular structures due to bonding of different…

Q: draw the 2 chair conformations of trans-1-bromo-3-isopropylcyclohexane

A: A trans isomer is one in which functional groups occur on opposite sides.

Q: How do I draw the most stable chair conformation for trans-1-ethyl-3-isobutylcyclohexane?

A: This question belong to Stereochemistry. Stable Conformation: More bulky group prefer equitorial…

Q: Looking alongC1−C2andC4−C5bonds, draw a Newman projection for each of the two chair conformations of…

Q: Draw the most stable conformations of cis-1,2-dimethylcyclohexane and trans-1,2-dimethylcyclohexane.

A: Conformational isomers: The conformational isomers are formed by the rotation of a carbon-carbon…

Q: Draw chair conformations of cis-1-ethyl-3-methylcyclohexane. Is one isomer favored over the other?…

Q: Draw both chair conformations of cis-1,2-dimethylcyclohexane. What is the H3C- C1-C2-CH3 dihedral…

Q: Draw the alternative chair conformation of this compound. Of the two chair conformations, which is…

A: Alternative chair conformation of this compound

Q: Draw the two chair conformations of the following substituted cyclohexanes. In each case, label the…

A: The compound is – cis-1-ethyl-4-isopropylcyclohexane.

Q: Use a Newman projection about the indicated bond to draw the most stable conformer for each…

A: A Newman projection, useful in alkane stereochemistry, visualizes the conformation of a chemical…

Q: draw most stable chair conformation of trans-1-tert-buty-3-methylcyclohexane and most stable chair…

A: Chair form Exist in stable and unstable forms stable form have least interaction while unstable…

Q: Is there a difference in the stability of the two cyclohexane conformations?

A: The structure of chemical compound can be represented as structural formula. A structural formula…

Q: Draw structural formulas for the cis and trans isomers of hydrindane. Show each ring in its most…

Q: 2D REPRESENTATION Cyclohexane Chair by stereoaisier H H H. .CH2 .H H' CH2 H. H V STAGGERED O…

A: Concepts of stereochemistry.

Q: Draw the most stable conformation of 1-chloro-3-isopropylcyclohexane and give its complete IUPAC…

A: The structure of 1-chloro-3-isopropylcyclohexane is as follows:

Q: Draw the alternative chair conformations for the cis and trans isomers of 1,2-dimethylcyclohexane,…

A: The planar form of cyclohexane is less stable due to the presence of high angle strain and hence it…

Q: Draw a Newman projection of the synclinal (or gauche) conformation of 1-iodo-2- nitroethane…

Q: Which has a higher percentage of the diequatorial-substituted conformer compared with the…

A: Cyclohexane consists of different types of confirmation. Disubstituted cyclohexane contains two…

Q: (a) Draw the most stable chair conformers of trans-1,3-diisopropylcyclohexane and…

A: Conformational isomers: The conformational isomers are formed by the rotation of a carbon-carbon…

Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

Draw the two chair conformations of each compound, and label the substituents as axial and equatorial of trans-1-ethyl-2-isopropylcyclohexane

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

Step 2

Step 3

ANSWER

Trending now

This is a popular solution!

Step by step

Solved in 4 steps with 7 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

Draw the structures of the two chair conformations of trans-1-tert-butyl-4-ethylcyclohexane. Which conformation is more stable? Explain your answer.
Draw the two chair conformations of cis-1-chloro-4-methylcyclohexane. Which of the conformers is more stable?
Draw the two chair conformations for t-butyl-cyclohexane and explain which is the most stable
draw the 2 chair conformations of trans-1-bromo-3-isopropylcyclohexane
Draw two different chair conformations of bromocyclohexane, showing all hydrogen atoms. identify each substituent as axial or equatorial. Indicate the most stable conformation.
Indicate the position, axial or equatorial, of the substituents in the more stable chair conformation. CH3 Methyl is [A] OH is [B] Isopropyl is [C] Cl is [D] HO` CI
NAME: 1. Draw the 2 chai conformations of cis-1-tert-butyl-2-ethylcyclohexane. Circle the most stable conformation of the molecule
The chair conformer of fluorocyclohexane is 0.25 kcal/mol more stable when the fluoro substituent is in an equatorial position than when it is in an axial position. How much more stable is the anti conformer than a gauche conformer of 1-fluoropropane, considering rotation about the C-1¬C-2 bond?
Describe the most stable conformation of each ring and compare these conformations with the chair conformation of cyclohexane.
5. Draw the two chair conformations ("ring filips") of trans –1- ethyl-4-methylcyclohexane to show the axial and equatorial substituents (including all hydrogens). Then determine which of the two conformations is more stable and why.
When cyclohexane is substituted by an ethynyl group, -C=CH, the energy difference between axial and equatorial conformations is only 1.7 kJ (0.41 kcal)/mol. Compare the conformational equilibrium for methylcyclohexane with that for ethynylcyclohexane and account for the difference between the two.
Draw the two possible ring puckers for trans-1,3-dimethylcyclobutane. Which of the two conformers is most stable? Why?