Arrange these halides in decreasing order of reactivity toward I- in acetone:
n-butyl bromide, sec-butyl bromide, tert-butyl bromide, allyl bromide, bromobenzene and benzyl bromide
Arrange these halides in decreasing order of reactivity toward I- in acetone: n-butyl bromide, sec-butyl bromide,...
Arrange these in order of decreasing reactivity with Ag+ and why. n-butyl bromide, sec-butyl bromide, tert-butyl bromide, allyl bromide, bromobenzene and benzyl bromide
1. arrange the halides in order of reactivity under the two
sets of conditions
Part 2: A Comparison of the Reactivity of Alkyl Halides 2% ethanolic silver nitrate 15 Nal in acetone 1. n-butyl chloride Clear Milky precipitate 2. sec-butyl chloride After heating, some precipitation 3. t-butyl chloride White precipitate After heating, precipitate Clear No precipitate Milk precipitate 4. n-butyl bromide Clear 5. allyl chloride White precipitate Brown color precipitate 6. chlorobenzene Clear Clear 1. Arrange the halides in order...
2.Data Table. Arrange the alkyl halides from Figure 3 in the order of expected reactivity (most reactive first) in EtOH/AgNO. Repeat the process for acetone/NaI. In both rankings, represent the molecules with both skeletal structures and name. Don't forget to include non-bonded electrons. D.OUTLA n-butyl chloride sec-butyl chloride tert-butyl chloride isobutyl chloride Вг. Br crotyl chloride n-butyl bromide ethyl iodide sec-butyl bromide
Arrange the alkyl halides in order of reactivity (from most to least reactive) under both SN1 (silver nitrate/ethanol) and SN2 (sodium iodide/acetone) conditions: 1-bromobutane, 2-bromobutane, bromocyclohexane, 2-bromo-2-methylpropane, 1-bromoadamantane, benzyl bromide, and bromobrmzene.
Arrange the following in order of decreasing reactivity
(fastest to slowest) toward electrophilic aromatic
substitution:
Arrange the following in order of decreasing reactivity (fastest to slowest) toward electrophilic aromatic substitution: COOH бо ob 6
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,...
Please order these alkyl halides from most to least reactive and
explain why structurally. Allyl chloride, n-butyl bromide,
n-butyl chloride, sec butyl chloride. They are reacted
with NaI and it is an Sn2 reaction.
Structures:
N-butyl bromide Allyl chloride Br | CV N-butyl chloride Sec-butyl chloride
III. Correctly arrange the compounds in each set in order of decreasing reactivity toward the indicated reaction (most reactive compound first). 1.Alkyl iodide formation with HI: A. 1-hexanol B. tert-butanol C. 2-pentanol D. isopentane Answer: __________ > __________ > __________ > _________. 2. Dehydrationwith catalyticH2SO4: A. cyclopentanol B. 2-methyl-2-hexanol C. methanol D. 1-octanol Answer: __________ > __________ > __________ > _________.
Halides tert-Butyl chloride 2-Chlorobutane 1-Chlorobutane 1-Bromobutane Bromobenzene Benzyl Chloride Crotyl Chloride Sy Read Lab Report Nucleophilie Substitution Reactions Section Date Name Part I. Sxl and S2 reactivity of different halides 1. Rank the seven halides from the most reactive to the least reactive in their Snl reactions. 2. Rank the seven halides from the most reactive to the least reactive in their SN2 reactions. 3. Write the complete chemical equations for the Syl and SN2 reactions that took place. Use...
Samples used: n-butyl alcohol, sec-butyl alcohol, tert-butyl alcohol, acetaldehyde, n-butyraldehyde, benzaldehyde, acetone, acetophenone, isopropyl alcohol Based on the samples used, which alcohol is most readily oxidized? Why d you think this is so?