Ans- Option 4
Explanation-
The general configurations for chair conformations are-
i.e if the substituents attached to 1 and 2 position are cis to each other, then one of them will be at axial and other will be at equitorial position in the chair conformation.
The same goes for (1,4) also i.e
Similarly other rules are-
So based on this for the given structures-
Which of the following could have both methyl groups in an equatorial orientation? CH CH, CH,...
5.5. Place the methyl groups by drawing the axial and equatorial positions on the cyclohexane structure in the chair conformations next to the cyclohexane derivatives named below. H H CH, H CH, CH, cis-1,2-Dimethylcyclohexane H CH, trans-1,2-Dimethylcyclohexane H CH, H CH, CH, eis-1,3-Dimethylcyclohexane CH, trans-1,3-Dimethylcyclohexane H H H CH, KO HC CH, cis-1,4-Dimethylcyclohexane н,с H trans-1,4-Dimethyleyclohexane
Identity which drawing of 1,2,3,4,5,6 hexamethylcyclohexane has all the methyl groups in adal positions, and which has all the methyl groups in equatorial positions Drag the appropriate drawings to their respective bins. The abbreviation for a methyl group, CH, is "Me". Reset Help all the methyl groups in equatorial positions all the methyl groups in axial positions
Q11. The correct structure of trans-1-bromo-3-methyl cyclopentane is ...Br (A) (B) -Br Br (C) (D) *Br Q12. The correct order of increasing stability for the following conformations is CH, H Н. Н H H H CH2CH3 H Н CH,CH CH CH3CH2 CH H2C CH, H CH, I II III (A) III < III (C) II <I<III (B) I<III <II (D) I< II < III Q13. Identify the relationship between the following two Newman projections. CH, H НАС. H Н;С. Н...
Which one of the following compounds will yield the indicated products below upon treatment with O3 followed by Zn/H+. H HC H H H H3C A) B) Q D) Which structure represents one of the resonance structure resulting from the compound shown below? HO. HO A) HO B) + C) HO. D) HO + HO E) Identify the type of reaction (CH3CH2)2Culi / THE H30+ A) Addition B) Rearrangment C) Elimination D) Substitution In the most stable chair conformation of...
Which compound can exist with two equatorial methyl groups? a) cis-1, 3-dimethylcyclohexane b) trans-1, 2-dimethylcyclohexane c) both a and b are true d) neither a nor b are true
12. Erythronolide B is the biological precursor of erythromycin, a broad-spel antibiotic. How many chirality centers does erythronolide B have? H-C A CH, нсон CH / O HC H30H ***OH CHE Erythronolide B a. 8 b.9 c. 10 d. 11 13. Consider the two methyl groups indicated with letters in the following molecular model. These two groups are: a. A: axial B: axial b. A: axial B: equatorial c. A: equatorial B: axiald. A: equatorial B: equatorial 14. Which of...
Question 1.) Which of the following describes the most stable conformation of trans-1-tert-butyl-3-methylcyclohexane? a.) Both groups are equatorial. b.) Both groups are axial. c.) none of these d.) The tert-butyl group is axial and the methyl group is equatorial. e.) The tert-butyl group is equatorial. Question 2.) Alkanes with one to four carbons exists as gases at room temperature. a.) True b.) False Question 3.) How many monochlorination products would be obtained from the chlorination of pentane a.) 1 b.)...
For each compound drawn below, label each OH, Br, and CH kroup as axial or equatorial. Be sure to answer all parts. Report problem Print Bro -- bH H Guided Solution с Но он 11 CH [3] HO h - H HI The axial groups in [1] are: a. OH D b. H Ос. Он а.н The equatorial groups in [1] are: а. ОН О Б . Н c. OH dH The axial groups in [2] are: e. Br D...
23) What is the following compound's systematic name? 23) CHE CH, CH CH,CHCH, A) 2-methyl-4-heptanone B)2-methyl-4-pentanone 2-methyl-4-hexanone D) 5-methyl-3-heptanone E) 5-methyl-3-hexanone 24) Which of the following is phenol? 24) CH2OH ОН I IV. op CH SO3H IT. III OCH A) B) IT D) IV E) V 25) 25) Which of the following substituents is a strong deactivator? A) -OCH3 B) -NO2 C)-COOH D) - E) none of the above
1 Determine the R/S orientation of the indicated chiral center(s) in the following molecules. If there is only one chiral center in the molecule, choose (none). H3C CH3 a Visited b H H3C Molecule #1 (B-thujene ): Center a: Center b: CH3 CH2 HO CH3 Molecule #2 ( rhodinol): Center a: Center b: CH3 OH CH, H3C CH3 H H H H CHE H H HO H CH3 H HO H 2-butanol OH CH3 CH a H b с The...