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
Arrange these in order of decreasing reactivity with Ag+ and why. n-butyl bromide, sec-butyl bromide, tert-butyl...
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
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
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
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?
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
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 immediately forms 2 layers with the Lucas test? Why do you think this is so?
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: __________ > __________ > __________ > _________.
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 the three metals (Zinc, Copper, Iron) and hydrogen in order of their decreasing relative reactivity and justify the order. Use symbols >, =, when appropriate. Briefly explain the basis of the order you selected.