Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations are not needed. Keep it short, brief, and direct because I only need the answers. The chair conformations of cis-1-tert-butyl-4-chlorocyclohexane is shown below? Which conformation is favored?

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: (c) Complete the template below to show the compound shown above in its chair conformation. Be sure…

A: Given is cyclohexane derivative

Q: CH3. H3C, H3C" HH CH3 Ring-flip H3C H3C H- -CI A B (A) A=1.0 kJ/mol; B=11.4 kJ/mol; difference =…

A:

Q: For each of the following disubstituted cyclohexanes, indicate whether the substituents in the two…

A: The axial and equatorial positions in chair conformation is shown below:

Q: 4. Draw the most and least stable conformations of the following substituted cyclohexanes in the…

A: For most stable chair conformation, the bulky group is attached to the equatorial position

Q: There are several rings in this structure. As highlighted in the middle diagram, the two explicit H…

A:

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: Which of the following statements is (are) true about cis- and trans-1,3-dimethylcyclohexane?

A: group at axial position faces 1, 3-diaxial interaction with hydrogen or any other groups at 3…

Q: Draw a Newman projection, similar to Figure 3-25, down the C1¬C6 bond in the equatorial conformation…

A:

Q: CI

A:

Q: H CI CI H H CI H CI A В (A) A and B are enantiomers. (B) A and B are diastereomers. (C) A and B are…

A: We are given two molecules, both have two chiral centers.

Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations…

A: The solution is as follows:

Q: The cyclohexane derivative shown exists primarily in the more stable of the two available chair…

A: Chair conformation is most stable of cyclohexane and groups are placed on respective equatorial and…

Q: CH3 CH3 CH3 CH3 H. H3C. .CH3 H. H3C. CH3 ČH3 CH3 ČH3 H3C- CH ČH3 H3C- H. ČH3 A B I-

A:

Q: A Newman projection of methylcyclohexane is shown below. Identify the which atoms will provide…

A:

Q: whether the more stable conformer (conformer B) of trans-1 can undergo E2 elimination. Thank you :)

A: Condition for E2-elimination -->stereochemical equipment is that ie the H which is abstracted by…

Q: CH3 H H3C- HZ H3C H CH3 A) They are enantiomers. B) They are diastereomers. C) They are…

A:

Q: In the space provided below, write a line structure corresponding to the systematic name…

A: Conformational analysis of 3-methylhexane . Stability based on  steric hindrance.

Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations…

A: The absolute configuration at two stereogenic centres of the newly discovered drug can be identified…

Q: The cyclohexane derivative shown exists primarily in the more stable of the two available chair…

A: Group a is at axial position. Group b is at equatorial position. Group c is at axial position.

Q: The cyclohexane derivative shown exists primarily in the more stable of the two available chair…

A: The given conformation is drawn as two chair confirmations as,

Q: The cyclohexane derivative shown exists primarily in the more stable of the two available chair…

A: Chair conformation is most stable and groups are attached on respective equatorial and axial…

Q: Explain why (1R,2S)-1,2-dibromocyclohexane is actually NOT a meso compound. Note make good…

A: Meso Compound   Meso compounds are generally achiral compound , but it also contains chiral centre.…

Q: CH2CH3 ring flip .CH2CH3 H3C ČH3 В A

A:

Q: The cyclohexane derivative shown exists primarily in the more stable of the two available chair…

A: All the three groups  are attached to the same face of the cyclohexane ring which means they are cis…

Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Draw the structure of the…

A: The solution is as follows:

Q: Between the cis and trans configuration of 1-chloro-3-methylcyclohexane, which is the most stable…

A: Groups which are axial in the chair form of cyclohexane derivatives cause instability in the…

Q: Draw the Sawhorse projection of the most stable conformer (boat/chair) of…

A: Ans- In sawhorse form, cyclohexane can be represented in two forms- 1) chair and 2) boat In which…

Q: 17. In the space provided below please draw (cis)1,3-dimethylcyclohexane in the most unstable chair…

A: Concept:  1) most unstable conformation meaning that the molecule will have higher energy & this…

Q: А. В. с. D. Е.

A:

Q: Sight along the C2–C3 bond of     2,3-dimethylbutane Draw a Newman projection of the most stable…

A: In Eclipsed conformation, atom or group of atoms are arranged in such a way that dihedral angle…

Q: 2, 3-Di-tert-butyl-1, 3-butadiene exists nearly exclusively in one conformation. What is the…

A: The given compound is 2,3-di-tertbutadiene. Since, it is an alkene it should have at least two…

Q: From the list below, assign the relationship to the following pairs of molecules, and circle any…

A:

Q: Determine the degrees of unsaturation from the compounds or formulas below. Click on the picture for…

A: Degree of unsaturation = (2C + 2 -H -X + N )/2 C= number of carbon atoms  H = number of hydrogen…

Q: Arrange the following four compounds in order of increasing boiling point, and briefly explain your…

A: The question deals with the concept of boiling point. it is defined as the  temperature at which…

Q: CH3 H, CH3 „CH(CH3) H CH; `CH3 `CH3 ČH(CH,)2 H' H `CH3 (H,C),HC А) A<B<C B) B<A<C С) С<A<В D) A<C<B…

A: General points to decide on the stability of the conformers: 1) Eclipsed &lt; Staggered 2) In…

Q: menthol HO A6 BI 4 DI 5

A: the number of possible stereoisomers for menthol are as follow.

Q: In the space provided below, write a line structure corresponding to the systematic name…

A: In line structure we use bond line notation.

Q: Br ОН CH3 doBr ОН a) and C2H5 CH3 C2H5 OH Br b) and „OH Br SCH3 SCH3 and Br Br d) and ()

A:

Q: CN and CN

A: Conformational sterioisomers wrt X and 2 hydrogens are the  Axial(Upwards) position which results in…

Q: Which cyclohexane chair, axial-methyl or equatorial-methy, is higher in energy and why? Draw the…

A: 1,3-Diaxial interaction is the repulsive interaction between an axial group and two axial groups or…

Q: HO OH HO OH HO OH OH HO. A в

A: Which of the following structures represents the enantiomer of compound X?

Q: 2. From the perspective of viewing down the C2-C3 bond, draw and name the Newman projection of the…

A: Newman projection is studied along the carbon-carbon axis and two carbon atoms are represented by a…

Q: Draw the most stable chair conformation of the cis-1-Ethyl-2-methylcyclohexane and estimate the…

A: The two possible chair confirmation of cis-1-Ethyl-2-methylcyclohexane are as follows: Among the…

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

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

Q: Draw out the most and least preferred chair conformation of the compound below. Draw their boat…

A: The number of stereoisomers of an organic molecule depends upon the number of chiral carbon atoms…

Q: For 1-ethyl-2-methylcyclopentane: draw all stereoisomers, and identify their stereochemical…

A:

Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations…

A: The solution is as follows:

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.