i will answer one question with explanation remaining direct answers is it ok?
12.
in chair conformation substitutents which are in axial position is less stable than equitorial position
because in axial position there will be 1,3 diaxial interactions are present
option A is correct answer
here both substitutentsa are in equitorial
13.
option C
in radical bromination teritiery hydrogen will go
14.
option B
15.
option B
COULD YOU ANSWER ALL 4 PLEASE Which is the most chair conformation of trans-1=ethyl-2-isopropylcyclohexane? 2.3-Dimethylbutane reacts...
Consider the four isomers of 1-ethyl-4-isopropylcyclohexane in a chair conformation. Which two chair conformations represent the trans isomers in equilibrium?
For trans-1-ethyl-4-isopropylcyclohexane, which two chair conformations are in equilibrium?
Draw the most stable chair conformation for trans-1-chloro-2-isopropylcyclohexane and please explain why its most stable Will Rate Correct Answers!!!!
1. The most stable conformation of trans-3-ethyl-1-iodocyclohexane is a. Et b. C. d Et Et 2. a 3. Which of the following is NOT a resonance structure of ozone? b. a. d. All are valid resonance structures C. 4. Arrange the following bicyclic alkenes in order of increasing stability (least stable to most stable) II II d. Il<lll< C. I<ll<llI b. I<lll<ll a. Ill<ll< 5 What is the correct Lewis structure for CHsNCO? b. No 0 НС H,C- a. d....
1. Draw the chair conformation for the following molecules: 이 2. Draw the most stable conformation for the following molecules: a) cis-1-ethyl-3-methylcyclohexane b) trans-1-tert-butyl-4-ethylcyclohexane c) (1R,2R,4S) 2,4-dimethyl-1-isopropylcyclohexane
Draw cis-1-ethyl-3-isopropylcyclohexane in its lowest energy conformation. -draw chair conformer in lowest energy conformation -include all of the hydrogens
Which of the following chair structures represents the lowest energy conformation of cis-1-methyl-2-isopropylcyclohexane?
Please show how to solve these questions! 1 The most stable conformation of trans 3-ethyl-1-odocyclohexane is: 2. List the following carbocations in the order of their stability (most stable first and least stable last). 6630 3. Arrange the following bicyclic alkenes in order of increasing stablity (least stable to most stable). 4. Assign the R and/or S configuration to the chirality centers in the following compound a) 2R, 3R b) 25, 3R c) 2R, 3S d) 25, 35 1. Provide...
Draw the most stable conformation for; a. trans-1-chloro-3-methylcyclohexane b. cis-1-ethyl-2-isopropylcyclohexane c. trans-1-bromo-4-ethylcyclohexane d. cis-2-bromo-1-methylcycclohexane Sppecifically, show the ring flipping and calculate the strain using the table given in the power point slides.
1. Rank the following carbocation intermediates in order of incrasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. 2. Rank the following free radical intermediates in order of increasing stability and draw important resonance forms when applicable. Classify each as primary, secondary, tertiary, allylic, or benzylic. CH2 bro ledo IV b III 10 112TV ] 21 3. 2,3-Dimethylbutane reacts with bromine in the presence of light to give a monobrominated product....