Draw both trans chair conformations of 2-methylcyclohexanol and circle the more stable one. Reduction of 2-MethylcyclohexanoneBackgroundIn this experiment, 2-methyleyclohexanone will be reduced to 2-methyleyclohexanol using sodiumborohydride.OHNalB,NaOHBOHwethanolwater

Answered: Image /qna-images/answer/0aa6bdfa-8816-4bb5-bb64-b4a08273e994.jpg

Answered: Draw both trans chair conformations of…

Science

Chemistry

Draw both trans chair conformations of 2-methylcyclohexanol and circle the more stable one.

Macroscale and Microscale Organic Experiments

7th Edition

ISBN:9781305577190

Author:Kenneth L. Williamson, Katherine M. Masters

Publisher:Kenneth L. Williamson, Katherine M. Masters

Chapter7: Extraction

Section: Chapter Questions

Problem 9Q

See similar textbooks

Related questions

Q: Draw the more stable chair conformation for the following compound. trans-1,2-dibutylcyclohexane

A: In Cyclohexanes chair conformation is more stable than boat conformation

Q: 1. Consider the molecule shown below. [1] Draw the two chair conformations for the compou [2]…

Q: Draw Newman Projections of the following molecule, looking down the C2-C3 bond. Under A, draw the…

A: Generally Anti conformer is most stable and eclipse conformer is least stable

Q: What chair structure corresponds to the highest energy conformation of trans-1,4-dichlorocyclohexane…

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: Draw the two chair conformations of cis-1-chloro-4-methylcyclohexane. Which of the conformers is…

Q: h) i) CH3CHSSCHCH3 CH3 CH3 Cl₂ [H] FeCl3 ?

A: h) Benzene reacts with Cl2 in the presence of Lewis acid FeCl3 to produce chlorobenzene. This…

Q: Draw the most stable conformation of cis-1-2-dimethylcyclohexane

A: The most stable conformation of cyclohexane is chair conformation. In chair conformation there is…

Q: Which of the following is the most stable conformation of the following compound? но. CI CI но. Но.…

Q: Given that pKa for phenol is 9.95 and pKą for the ammonium ion is 9.24, will the following reaction…

A: Since, you have asked multiple questions then we will solved first question for you by details…

Q: Shown is one isomer of 2,4-dibromo-1,3,5-triethylcyclohexane. Draw both chair conformations of this…

Q: Order the conformations of butane from lowest energy to highest energy (1 being the lowest energy).…

A: Dihedral angles measure the angle between 2 given substituents on different carbons in a Newman…

Q: Draw cyclohexanol in its chair conformation with the functional group in both its axial and…

A: The conformational isomers are formed by the rotation of a carbon-carbon single bond in a…

Q: Given the wedge and dashed conformers of butane, classify each conformation. H3C H3C H3C . CH3 ""CH3…

A: The given conformations of butane are in wedge and dash form, they need to be converted into Newman…

Q: 2 Draw a Newman projection for the Tolowing compound as viewed down the indicated bond in the…

Q: 5. Draw the two chair conformations ("ring flips") of trans –1-ethyl-4-methylcyclohexane to show the…

Q: Which structure represents the lowest energy conformer of trans-1-ethyl-2-methylcyclohexane? A. B.…

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

Q: 5. Draw the most stable chair conformation of the given trisubstituted cyclohexane? Br

A: Answer of this question:- The most stable chair confirmation is:-

Q: 1. Draw the 2 chai conformations of cis-1-tert-butyl-2-ethylcyclohexane. Circle the most stable…

Q: a) Draw the chair conformations of 1, 4 – ditertbutyl cyclohexane. b) Determine the most stable and…

A: The given compound 1,4-ditertbutyl cyclohexane has cis and trans isomers. The structures of cis and…

Q: Starting from the Newman projection below, rotate the back carbon to provide the structure in the…

A: For given question there is need to determine least stable Newman projection of following compound.

Q: What is the energy difference between the axial and equatorial conformations of cyclohexanol…

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

Q: mpare the follov nformers Of opropan-1-Ol. tch each con to ir corresponding relative energy. Recall,…

A: Interpretation : We have to arrange the following in according to its energy.

Q: Draw the most stable conformation of the following molecules. Label the groups as axial and…

A: Conformation is spacial arrangement of atoms which can be converted into one another by rotation…

Q: Is 2-methyl-prop-1-ene symmetric? Please explain why with emphasis on the hybridization of each…

Q: CH3 CH, CH H,C. *CH3 H,C

Q: Starting from the Newman projection below, rotate the back carbon to provide the structure in the…

A: Here, most stable conformer means that conformer which has minimum potential energy. Right now, it…

Q: Starting from the wedge-and-dash structure below, rotate the back carbon to provide the Newman…

A: Dihedral angle in Eclipsed conformation is zero degree and so this conformation have large steric…

Q: Please help me with this question

A: The axial and equatorial positions in chair conformation of cyclohexane are as,

Q: According to the following structure, draw the Newmann projections in which you must indicate: a)…

A: The Newman conformation of the given structure is

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

100%

Draw both trans chair conformations of 2-methylcyclohexanol and circle the more stable one.

Reduction of 2-Methylcyclohexanone
Background
In this experiment, 2-methyleyclohexanone will be reduced to 2-methyleyclohexanol using sodium
borohydride.
OH
NalB,
NaOH
BOH
wethanol
water

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

Step 3

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 3 steps with 3 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

how to synthesize 2-phenylclohexanone from cyclohexanone?
Which would be the best reagent to convert benzaldehyde to benzoic acid? O PCC KMnO4 NaBH4 OLIAIH4
ČOEt 1. EtO-Na+ OEt 3. NAOH, H,O, heat EtO 4. HCI, heat 2-Carbethoxy- 4-Butanolactone 4-butanolactone (y-Butyrolactone) Show how the scheme for formation of 4-butanolactone can be used to synthesize lactones (a) and (b), each of which has a peach odor and is used in per- fumery. As sources of carbon atoms for these syntheses, use diethyl malonate, ethylene oxide, 1-bromoheptane, and 1-nonene. (b) (racemic) (racemic)
Acetal and Hemiacetal formation: c. Acetal/hemiacetal CH 3 ty CH H3C [ a. hemiacetal H3C d. Cyclic hemiacetal Gyertych OH Esterification/Amidation: e. Fisher esterification OH + CH₂OH + H3C CH3 H OH + CH3OH H [H*] H₂SO4 H™ a. hemiacetal b.acetal + H₂O
Select the best answer. Briefly explain the selection. A mechanism is an acceptable explanation.
In the synthesis of methyl m-nitrobenzoate from methyl benzoate using HNO3 and H2SO4 via EAS the product is washed with ethanol to remove impurities. By impurities do they mean o-nitrobenzoate and methyl p-nitrobenzoate? How come ethanol can remove o-nitrobenzoate and methyl p-nitrobenzoate, but has no effect on m-nitrobenzoate? Thank you.
one hemiacetal and one acetal bond in the following dissacharide. Please them and indicate which kind of bond it is. H. Н ОН OHO HO H- H. H. H. ОН OH H. H- -H- H. H. OH ОН
From the table of available reagents select the one(s) you would use to convert 1-phenylethanol to l-phenylethanethiol Use the minimum number of steps; in no case are more than four steps necessary. List reagents by letter in the order that they are used; example: fa. Reagents available .CO3H a. CH3B. e. H30* i. b. HCI f. NaH c. Hg(OCOCF3)2, (CH3)2C=CH2; then NABH4 g. PBR3 h. POCI3, pyridine j. (CH3)3COH d. (H2N)2C=S; then "OH, H2O
what are the products of the following reactions? trace amt, acid is present) (a a) Cyclopentanone + cyclohexylamine b) 3-pentanone + butylamine C)3-pentaname + Cyclohexyamine
14-1:
What sequence of steps can comvert benzene into 4-isobutylacetophenone
Why do we react β-naphthol with ethyl iodide rather than react ethyl alcohol with 2-Iodo naphthalene? Draw out a putative mechanism for ethyl alcohol reacting with 2- Iodo naphthalene and explain why this method wouldn’t work