Answer is C).
Most stable structure is one which contain negative charge on Electronegative atom (oxygen ) and positive charge on electropositive atom which is II. Least stable structure is one with positive charge on Electronegative atom (oxygen) which is I.
SE ATO 1800A . Rank the following resonance structures from MOST to LEAST stable a. III...
Rank the following radicals in order of decreasing stability (most stable to least stable 11 III TV III > I > I > IV III > | > | > IV Ill > IV> || >1 IV>]> || > III II >> III > IV
Rank the following radicals in order of decreasing stanility (most to least stable) II IV IV > I > II > III III > II >> IV III >> II > IV Il > III > I > IV III > IV > Il > 1
What is the IUPAC name of the following compound? 4 Rank the following alkenes from most to least stable. ОН OH ОН IX M A. I > || > III B. I > III > 11 C. II > III > 1 D. III > II > Which carbon would form the most stable carbocation? A D В С Which of the following is a wax at room temperature? A. B. C. D. E. None of these
Question 8 (1 point) ІІ. Т Rank the carbocations above from most to least stable. O III>II>I O II>>II OI>> Ош>.
QUESTION 24 Rank the following carbocations in order of stability. (The most stable is first.) T> III > 1 all > > II T>ll> 111 ll>I> III
Need help understanding why? Thanks! 9. Rank the following from most to least acidic CI COOH COOH coOH COOH IV A. I II III >IV B. II I IV> III C. III IV II > I D. IV III I > II E. III IV I II 10. Which hydrogen is the most acidic in the molecule shown below? C A 11. Why are ketones less reactive than aldehydes? A. Ketones are less sterically hindered. B. Carbonyl carbon of ketones...
Rank the following carbocations in order of increasing stability. CHCI CH -CHCI C–CH CH C1 CH I II III a. (least stable) I < II < III (most stable) b. (least stable) II < I < III (most stable) c. (least stable) III < I < II (most stable) d. (least stable) III < II < I (most stable) e. (least stable) I < III < II (most stable) f. (least stable) II < III < I (most stable)
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
2. Carbocation stability: Rank the following carbocations from the most stable to the least stable. + (a) (b) (c) (d)
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?