III. Correctly arrange the compounds in each set in order of decreasing reactivity toward the indicated...
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: __________ > __________ > __________ >
_________.
Homework Answers
![3.- chain carbocation C. Methanol, CH2-OH . eation formed, CHED I cation D. L-oetanot; CH2 CM2]c-CH3 ; cation formed; methyl](http://img.homeworklib.com/questions/731d5e10-b042-11ea-a3f0-73b2dfaacc90.png?x-oss-process=image/resize,w_560)
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III. Correctly arrange the compounds in each set in order of
decreasing reactivity toward the indicated...
Arrange the following compounds in order of decreasing reactivity as electrophiles. From the most reactive to...
Arrange the following compounds in order of decreasing reactivity as electrophiles. From the most reactive to the least reactive. NH2 Br D A B. с Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a D>C>BA b D>B>CA c A>B>C>D d D>A>>B 2.) Aa N Р х W
Arrange the following compounds in order of DECREASING reactivity with Hoffor HORATE 51 is the MOST...
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
Arrange these halides in decreasing order of reactivity toward I- in acetone: n-butyl bromide, sec-butyl bromide,...
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
Question 2 4 pts Rank the following compounds in order of decreasing reactivity toward nudeophilic attack,...
Question 2 4 pts Rank the following compounds in order of decreasing reactivity toward nudeophilic attack, by inputing a ranking number (1-4) in the box next to each structure (most reactive-1).
Testbank, Question 029 Arrange the following compounds in decreasing (highest to lowest) order of boiling point....
Testbank, Question 029 Arrange the following compounds in decreasing (highest to lowest) order of boiling point. 1-pentanol hexane 1-pentanamine butyl methyl ether IV III>I>IV>II >III>IV>11 >IV>III>II >II>II>IV III>I>II>IV here to search o et e a F F4 F5 F6 FB #
Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reactions (most...
Rank the following compounds in order of decreasing reactivity
in a nucleophilic acyl substitution reactions (most to least
reactive from left to right in the answer)
yucuruit pun Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reaction (most to least reactive from left to right in the answer): ei ole C>A>D>B A>C>D>B A>C>B>D C>A>B>D
2.Data Table. Arrange the alkyl halides from Figure 3 in the order of expected reactivity (most reactive first) in...
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
Spid deri 7. What is the order of DECREASING reactivity toward nucleophilic acyl substitution for these...
Spid deri 7. What is the order of DECREASING reactivity toward nucleophilic acyl substitution for these carboxylic acid derivatives (most reactive first)? 9. Using your knowledge of organic chemistry, what is the order from most reactive to least reactive of these esters toward a nucleophile? och la NHCH I NHCH 1 2 (a) II, IV, III, I (b) I, II, III, IV (a) 1 > 2 > 3 (b) 3 >1 > 2 (c) 2 > 3 > 1 >2...
Arrange the following groups of compounds in order from most reactive to least reactive toward electrophilic...
Arrange the following groups of compounds in order from most reactive to least reactive toward electrophilic aromatic substitution. 1. Benzene, ethylbenzene, chlorobenzene, nitrobenzene, anisole. 2. Toluene, p-cresol, benzene, p-xylene. 3. Benzene, benzoic acid, phenol, propylbenzene. 4. p-Methylnitrobenzene, 2-chloro-1-methyl-4-nitrobenzene, 1-methyl-2,4-dinitrobenzene, p-chloromethylbenzene.
Arrange the alkyl halides in order of reactivity (from most to least reactive) under both SN1 (silver nitrate/ethanol)...
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 compounds in order of decreasing reactivity as electrophiles. From the most reactive to the least reactive. NH2 Br D A B. с Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a D>C>BA b D>B>CA c A>B>C>D d D>A>>B 2.) Aa N Р х W
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
Question 2 4 pts Rank the following compounds in order of decreasing reactivity toward nudeophilic attack, by inputing a ranking number (1-4) in the box next to each structure (most reactive-1).
Testbank, Question 029 Arrange the following compounds in decreasing (highest to lowest) order of boiling point. 1-pentanol hexane 1-pentanamine butyl methyl ether IV III>I>IV>II >III>IV>11 >IV>III>II >II>II>IV III>I>II>IV here to search o et e a F F4 F5 F6 FB #
Rank the following compounds in order of decreasing reactivity
in a nucleophilic acyl substitution reactions (most to least
reactive from left to right in the answer)
yucuruit pun Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reaction (most to least reactive from left to right in the answer): ei ole C>A>D>B A>C>D>B A>C>B>D C>A>B>D
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
Spid deri 7. What is the order of DECREASING reactivity toward nucleophilic acyl substitution for these carboxylic acid derivatives (most reactive first)? 9. Using your knowledge of organic chemistry, what is the order from most reactive to least reactive of these esters toward a nucleophile? och la NHCH I NHCH 1 2 (a) II, IV, III, I (b) I, II, III, IV (a) 1 > 2 > 3 (b) 3 >1 > 2 (c) 2 > 3 > 1 >2...
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