https://juexams.com/moodle/mod/quiz/att-Time letThe most stable conformation ofcis-l-isopropyl-2-methylcyclohexane will have:ut ofO a. both groups axialb. groups at opposite sides of ringc. methyl equatorial, isopropyl axiald. both groups equatoriale. methyl axial, isopropyl equatorialNext p-Nevt acthp

In the most stable conformation of Cis-1-isopropyl-2-methyl cyclohexane the methyl group is at axial…

The most stable conformation of cis-l-isopropyl-2-methylcyclohexane will have: O a. both groups axial b. groups at opposite sides of ring c. methyl equatorial, isopropył axial d. both groups equatorial e. methyl axial, isopropyl equatorial

The most stable conformation of cis-l-isopropyl-2-methylcyclohexane will have: O a. both groups axial b. groups at opposite sides of ring c. methyl equatorial, isopropył axial d. both groups equatorial e. methyl axial, isopropyl equatorial

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter6: Alkanes & Alkenes

Section: Chapter Questions

Problem 8CTQ

See similar textbooks

Related questions

Q: CH2CH2CH3 CH2CH2CH3 CH2CH2CH3 CH2CH2CH3 CH2CH2CH3 CH2CH3 H H. F CH2CH3 F H-H H3CH2C- H. H' H. H. F…

A: here you ask question (a) to (f), but i can see only question (d) to (f) so, I am solving question…

Q: Q2. a) Draw the Newman projection of the most stable staggered conformation of 2-methylpentane,…

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: hat is the most stable chair conformation form of trans 1 -tert-butyl -3-methylcyclohexane? a)Axial…

Q: Which conformation in each pair is higher in energy? Calculate the energy difference between the two…

A: When atoms are rotated around a single bond in a three-dimensional arrangement, the resulting…

Q: Place the conformations of cis-1-isopropyl-4-methylcyclohexane that are drawn below in order of…

A: - Most stable comfomation of cyclohexane is the Chair conformation - it follows following order…

Q: Rank the following conformations in order of increasing stability. The first conformation in your…

A: Conformations of a molecule means their different arrangements in space. For eg. Humans have…

Q: the wedges are supposed to be up, but why the both chair comformations point down? CH3 CH3 H3C CH3…

A: Two types of bonds exist in cyclohexane chair conformer. Axial and equatorial. When only a single…

Q: Explain why1-bromobicyclo [2.2.2] octane is not likely to undergo an SN1 or an Sn2 substitution…

A: No SN1 or SN2 reaction is likely to undergo for 1-bromobicyclo[2,2,2] octane . In the SN1 reaction,…

Q: n the ortho position in chlorobenzene. CI chlorobenzene • You do not have consider stereochemistry.…

Q: bon #1 and #2. Let the carbon #1 containing the methyl group to front while carbon #2 containing the…

Q: Newman

Q: Can you show the calculation and how did you decide how many of CH3-H you will calculate

Q: Given the planar trisubstituted cyclohexane below, fill in all boxes (with H, Cl or Br) to complete…

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

Q: 1) Use conformations A and B shown below to answer the following questions. Br. H Br H H H H H H CI…

Q: Rank the following carbocations in order of increasing amounts of hyperconjugation. The first in…

A: The amount of hyperconjugation depends upon the number of hydrogen atoms on the adjacent carbon to…

Q: %3D and cis trans Explain why cis-bicyclo[4.1.0]heptane is more stable than its trans isomer.…

A: The solution of the answer is given below:

Q: 8. What is the correct order of stability, starting with the most strained, for the conformations…

Q: sawhorse projection of the following structure (1,2-dibromopropane) in a conformation in а. which…

Q: Draw the conformational isomers of 1-bromo-2-chloroethane by rotating C-C single bond with dihedral…

A: The conformational isomers are obtained by the interconversion of the single bonds present in a…

Q: 3. (20) Cyclohexane may go through ring-flipping as shown below. 5 (a) Draw both of the possible…

Q: Part B: Newman projections. 1. Construct a model of the provided molecule (match the configuration…

A: More unstable conformer having higher value of gibbs free energy. Usually eclipsed conformation is…

Q: Rank the following carbocations from least to most stable: I. I. III. IV. III. < |I. < IV. < I. O…

Q: Which compound(s) is(are) secondary haloalkane(s)? H CH3 CH3 CH3-C CH3 CH3-C CI CH3-CH2-CH2 Br…

A: Secondary haloalkanes are those compounds in which halogen attached to carbon is further atteched…

Q: Which substituent Z will help the most to active the benzene ring? HNO, H,SO, (а) -Br (b) -C(CH3)3…

Q: Rank the molecules below from least stable to most stable

A: we have been asked the stability of given ring structure

Q: b) Draw the Newman projections of all conformations of this haloalkane looking down the indicated…

Q: 2. Draw the most stable conformation of the following: (a) trans-1-butyl-3-methylcyclohexane (b)…

A: Bulky group should be present at equitorial position for stability so that it can feel minimum…

Q: Which Newman projection of 2-methylbutane represents the least stable conformation of the compound?…

A: If both the groups are 180o to each other in different carbon atom then it is called staggered…

Q: Chapter 4 - Chair and Boat conformations of cyclohexane, mono-, di- and tri- substituted cyclohexane…

A: Conformation- Shape adopted by the molecules caused by rotation around one or more single bond is…

Q: can this be explained please with full and understandable explanation

Q: Represent in perspective the most stable conformer of trans-4 isopropylcyclohexan-1-ol.

A: When Trans 1,4 disubstituent's come into scene. Its always axial-axial or equatorial-equatorial. If…

Q: down Lescagon (dashrwedn? 3. Provide the hexagon structure for -1,4-ditert-butylcyclohexane. Also…

Q: Estimate the relative stabilities of the 4 conformations eclipsed and eclipsed n-pentane by drawing…

A: Since you have posted multiple questions, we will answer only first question for you. If you want…

Q: Dr@w the chair conformation and its ring-interconversion isomer of both cis and…

A: Given molecule is 1-cyclobutyl-2-methylcyclohexane. The conformation in which More bulky group is…

Q: Which is the least stable conformer of pentane? H. H H H CH₂CH₂ H CH3 AMA CH₂CH3 H AYA RAT FIR AYA…

Q: CH3 H (+) H;C-C-CH3 H,C-g-CH, CH3 H3C-CH2 А. С. D. B.

A: In this question, we will Select the most stable carbocation. You can see details explanation and…

Q: Explain with appropriate chair structures why cis-decalin (ie. cis-bicycle[4.4.0]decane) is only…

Q: 1. Draw the product of the reaction below: H* CH;CH,CH,C-H + CH;CHOH CH3 2. Draw the product of the…

A: The reaction of an aldehyde with alcohol in presence of acid leads to the formation of a hemiacetal…

Q: Draw the most stable conformation of the disubstituted cyclohexane below

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

Q: (a) Draw all stereoisomers formed by monochlorination of the cis and trans isomers of…

A: (a) The stereoisomers of all the monochlorinated products of cis-1,2-dimethylcyclobutane are shown…

Q: CH, CH3 CH2 - CH2 - CH-CH CH3. CH3 CH3 CH3 CH3 CH Least stable elipsed configuration Most Stable H…

A: Yes you are true Eclipsed form is if dihedral angle is 0° between group If dieheadral angle is 60°…

Q: (a) Draw all stereoisomers formed by monobromination of the cis and trans isomers of…

A: We are given to draw the stereoisomers of cis and trans isomers of 1,2-dimethylcyclohexane.

Q: What is the energy difference between the staggered and eclipsed conformations of…

Q: What is the most stable chair conformation of the 4-methoxy-1,2- dimethylcyclohexane structure given…

A: Given: 4-methoxy-1,2-dimethylcyclohexane To find: Most stable chair configuration Solution:…

Q: II CH3-CH2-CH2-CH Butanal CH3 CH3 CH2 CH3 0 II CH3-C-CH,– CH3 CH2-CH CH3-CH-CH CH2 =C- CH3 A B D

A: The structure that is not an isomer of butanal has to be determined.

Q: Br A. A B. B Select the most stable conformation of 3-bromo-2-methylpentane, viewed through the…

A: ->the conformer in which bulkier group are opposite to each other are most stable.

Q: Illsutrate the Ring-flipping interconverts axial and equatorial hydrogens incyclohexane ?

A: Cyclohexane- Structure is- In the conformational analysis cyclohexanes, cis and trans isomers…

Q: Pentyl butane Accurate 2- (1- methylethyl) Impacible Bicyclo propane Accurate Cycloethy! Impossible…

Q: Which conformer of pentane is the least stable? CH CH2CH3 CH,CH, CH3 CH2CH3 H. HCH,CH3 H. H. CH H'…

A: In the Newman projection , when the bulky substituents are Anit staggered to each other , this is…

Q: For the compound below please identify the position of equilibrium (which chair conformation is more…

A: Given : Structure of molecule.

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

https://juexams.com/moodle/mod/quiz/att-
Time let
The most stable conformation of
cis-l-isopropyl-2-methylcyclohexane will have:
ut of
O a. both groups axial
b. groups at opposite sides of ring
c. methyl equatorial, isopropyl axial
d. both groups equatorial
e. methyl axial, isopropyl equatorial
Next p-
Nevt act
hp

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

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps with 1 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

a model of cyclohexane in a chair conformation, and explain why the names “axial” and“equatorial’ are appropriate.
Two conformations of cis-l, 3-dimethylcyclobutane are shown. What is the difference between them, and which do you think is likely to be more stable?
Build a model of methylcyclohexane, and use the model to complete the following Newmanprojections of methylcyclohexane in the chair conformation: a. When the methyl group is in an axial or equatorial (circle one) position, the molecule is inits lowest potential energy conformation. b. Label one Newman projection above anti and the other gauche to describe the relationshipbetween the methyl group and C3 of the ring. c. In general, which is a lower PE conformation, anti or gauche? d. Explain how your answer to b and c provide an explanation for why it is more favorable fora large group to be in an equatorial than an axial position.
Indicate the relationship between each pair. Choose from: configurational stereoisomers,conformers, constitutional isomers, or different formulas (Each term is used at least twice.)
Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.
attatched below are heterocyclic problems for practice. Please assist me
What is the product (A, B, C, or D) of the reaction shown in Image30? a. C b.D c. B d. A
By considering the stereochemical requirements for E2-elimination, and using an appropriate illustration need help indicating whether the more stable conformer (conformer B) of trans-1 can undergo E2 elimination. Thank you :)
iupac nme include stereochemistry if ncessary
Please advise: is model of the (E) 2-bromo-2-butene has its priority numbers of each substituent labeled correctly. I also, belive this is a E-isomer. Justin
Question 5: Conformations The elimination shown below has a very large differenco in the rate of reaction that depends on the stereochemistry of the substrate. Please use chair conformations in the space below to explain the results shown in the box. Please provide a brief explanation of the observed reactivity difference in the second box. Chair conformations:
For each of the following molecules draw the most stable conformations indicated in the parenthesis, and along the specified bonds.a) sec-butylcyclohexane (Newman projection chair along C1-C2 and C5-C4)