Correct order is D > A > C > B.
D and A ate staggered whereas C and b are eclipsed.
In case of D both carboxylic groups are opposite to each other. No interaction at all. Hence more stable.
In case of A, both carboxylic groups shows gauche interaction. Hence less stable compared to D.
In case of B, both carboxylic groups shows eclipsed interaction with each other. Hence highly unstable.
In case of C, both carboxylic groups shows eclipsed interaction with H. Hence more stable compared to B.
Order the following compounds from most to least stable. HOC CO,H нсон HO,C -CO,H COH B,...
What is the relationship between the following compounds? O H H HO HO- HOC CH3 CH3 Enantioners Diastereomers Identical molecules Geometrical isomer What is the relationship between the following compounds? HOME HOyC..., COZH COH Enantiomers Diastereomers Identical molecules Geometrical Isomers
Which diene and dienophile would react to give the following Diels-Alder product? .COH "COH LCOH HOC + Y COH H0_C_ HO₂G Coah COH CO + HO,C-=-CO,H + HOẠC_COH
1) Rank the following compounds in order from most stable to least stable. Explain your reasoning. D¢?? A. 1 > 2> 3>4 B. 1>2>4> 3 C. 4>1>2>3 D. 4>3>2>1 E. 2 >4 >1>3
Rank the following allylic carbocations in order from least stable to most stable THEN justify your answer in words: For each of the following pairs of compounds, circle the one that is the stronger acid: Which one of the following is the MOST stable carbocation? Circle the correct answer.
2. Rank the following carbocations in order from least stable to most stable THEN justify your answer thoroughly in words A B C D
Put the following C-H bonds in order of which one would lead to the most stable radical. If the C-H bond forms a more stable radical, then the bond strength will be weaker. 5) Put the following C-H bonds in order of which one would lead to the most stable radical. If the C-H bond forms a more stable radical, then the bond strength will be weaker. HE most stable radical weakest C-H bond least stable radical strongest C-H bond...
Rank the following phenolic compounds in order of acidity Least acidic Most acidic HO HO O H0 CI HO N. 0
Rank the following alkenes from most stable to least stable. C > A > B A > C > B B > A > C B > C > A C > B > A A > B > C
order the following carbon radicals from most stable to least stable (1&2) 1. Order the following carbon radicals from most stable to least stable. 5 3 2 2. Complete the following reaction scheme. "What goes over the arrow?" Write your answers in the spaces provided below. MgBr Br E Br ОН MgCl CI F G В Н Br Reagents required for the above reactions: F. А. G. В. Н. С. I. D. J. E. (
Rank conformations bcd from most stable to least stable (most stable first) DUH ΤΗ HH Conformation A Question 2 (1.5 pts] Rank conformations B, C and D from most stable to least stable (most stable first C(CH.CH2CH3)3 CH(CH3)2 X H H H HH А Conformation B Conformation C Conformation D Question 3 (1.5 pts) Which one of the following statements about structure E is correct?