2. Arrange the following in order of: (i) increasing reactivity with HCI. CH, CH CH H.C=C...
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...
Please explain your reasoning for the correct answer also Arrange the following in order of increasing stability CH2CH3 CH3 CH CH CH CH,CH, most stable least stable. Arrange the following in order of increasing stability CH2CH3 CH3 CH CH CH CH,CH, most stable least stable.
18, 3(b) Arrange the following alcohols in terms of their increasing reactivity when treated with hydrogen halides. Also write which is the most and least reactive. ROH + H-X RX - HOH CH3 'ÇH3 CH3 CH₂ - CH2-OH CH₃OH CH₃ -CH₂OH Citz-c -OH Ct3
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...
Arrange the following compounds in order of DECREASING reactivity with Hoffor HORATE 51 is the MOST REACTIVE and 4 is the LEAST REACTIVE) CH,CH, CCH (CH), CHOCH Tonyo, onde on, ouder, CH, CH bor
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 haloalkanes in order of increasing reactivity in an Sn2 reaction with NaI in acetone (least first). a. Methyl bromide b Isopropyl chloride t-butyl iodide d. Isobutyl chloride aus CH3 cиз C. Arrange the haloalkanes in order of increasing reactivity in an SN2 reaction with Nal in acetone (least first). CH3 - CH2CH2-I C-Br CI Br CH3 I 11 II IV I, IV, III, II b II, II, I, IV a. IV,I, II, II с. d. III, II, IV,...
2. (13 pts) Use the letters A, B, and C to arrange the items in each group according to the property indicated. a. Basicity: Strongest Base Weakest Base A. HCEC B. H2N C. CH30 b. Reactivity in SN 1 Reactions: Most Reactive Least Reactive A. Br c. Reactivity with Bra/FeBrs: Most Reactive Least Reactive d. Stability: Most Stable Diene Least Stable Diene А, не в. но CH, C. HO C H сн -C=C н сн, ċ-CH₂-C нс CH e. Stability:...
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 <...
Problem 6.3 Arrange these carbocations in order of increasing stability. CH, () CH (c) CH2 3