Arrange the following weak bases in order of expected increasing stability. Η Ο HH H-C-0- H-0-0-...
help? Arrange the following weak bases in order of expected increasing stability. Η Ο H' H-C d! : - H-C-0-0 H-0- H I II a. (least stable base) III < II < I (most stable base) b. (least stable base) II < III < I (most stable base) c. (least stable base) I < II < III (most stable base) d. (least stable base) III < I < II (most stable base) e. (least stable base) I < III <...
Arrange the following weak bases in order of expected increasing stability. H CH CH3 H-C-H HC-N-CH, HỌC-C-CH, * *0 II III a. (least stable base) III <I < II (most stable base) b. (least stable base) I < II < III (most stable base) c. (least stable base) III <II < I (most stable base) d. (least stable base) I III < II (most stable base) e. (least stable base) II < 1 < III (most stable base) f. (least...
Rank the following carbocations in order of increasing stability. CH-C1 CH; C -CH-CT o C -CH3 CH-Cl CH; ܚ II INI a. (least stable) II < III < I (most stable) b. (least stable) I III < II (most stable) c. (least stable) III < II < 1 (most stable) d. (least stable) III III (most stable) e (least stable) I II III (most stable) (cast stable) III III (most stable) Arrange the following weak bases in order of expected...
( 4 ) Arrange the following carbocations in the order of increasing stability (least stable first). СНа OC-CHE H-C-H N - a) IV, I, III, II b) III, I, IV, !! c) III, IV, II, 1 d) I, II, II, I
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)
Arrange the following radicals in order of increasing stability (least stable to most stable) Arrange the following radicals in order of increasing stability (least stable to most stable). Least stable Most stable
Arrange the following three bases in order of increasing base strength. NH CH3OH ОСН; II I III a. (Weakest base) I < II < III (Strongest base) b. (Weakest base) I < III < II (Strongest base) c. (Weakest base) II < I < III (Strongest base) d. (Weakest base) II < III < I (Strongest base) e. (Weakest base) III < II <I (Strongest base) f. (Weakest base) III < I< II (Strongest base)
H Arrange the following molecules from lowest to highest boiling point. H Η Η H-C-0-C-H 1-0 H-c-c-0-H Η Η (1) (II) H H Η Η H-0---0-H II Η Η Η Η Η H-c-c-c-H T Η Η Η (IV) Ο Ν < | < | < III Ο Ν < | < | < | Ο | < | < | < IV Ο | < | < ΠΙ < IV
2. Arrange the following in order of: (i) increasing reactivity with HCI. CH, CH CH H.C=C nec nec 20 cm H.C=C CH HC=C CH, (b) H.C=C NHCH, CHOCH, ОСН, (a) (c) (d) Teast reactive most reactive (ii) increasing stability. CH CH3 CH (a) (C) least stable most stable (iii) increasing heat of hydrogenation. CH,CH, CH=CH2 C H.CH O CH.CH CH3 CH,CH; CH,CH, (0) lowest heat of hydrogenation
Arrange in order of increasing stability. Label most and least stable. Show your work and explain why! Thank you. b) sots) Arrange in order of increasing stabilit most stable" an ea SM S CHS H C CH