2. Rank the following compounds in order of increasing rate for nitration with 1 most reactive....
Rank the compounds below in order of increasing rate of
electrophilic aromatic nitration.
CH3 0CH:
6. Circle the aromatic compounds from the list below. (5
points)
7. Rank the compounds below in order of reactivity to
Electrophilic Aromatic Substitution. Rank the most reactive
compound as compound 1 and the least reactive compound as compound
5. (5 points)
6. Circle the aromatic compounds from the list below. (5 points) OH :O: H 7. Rank the compounds below in order of reactivity to Electrophilic Aromatic Substitution. Rank the most reactive compound as compound 1 and the least...
3. Rank the following compounds in order of increasing rate of bromination from 1 to 5 (i.e., from 1 for least reactive to 5 for most reactive). ОН ОН ОН ОН ОН CH3 Br NO2 NO2 CH3 $ de represente en & NO2 - ii iv V iii iv 4. Which of the following compounds can probably be prepared in a good yield (as a major product) from benzene using two successive electrophilic substitution reactions? Check all that apply. Br...
3. (i) Rank order the following compounds with most reactive at top and most stable at the bottom. (ii) Provide a name for each functional group. (iii) Indicate how to make each functional group beginning with a carbonyl compound (e.g., phosgene, or the carboxylic acid or derivative thereof) and amine or alcohol or thiol. ROR RN-R I-z 0 Ann-R' Ron I-Z H H
H 7. Rank the compounds below in order of reactivity to Electrophilic Aromatic Substitution. Rank the most reactive compound as compound 1 and the least reactive compound as compound 5. (5 points) NO2 pada CH SO3H OH 5
Question 3 0.6/1 point Rank the following compounds in order of increasing rate of bromination from 1 to 5 (i.e., from 1 for least reactive to 5 for most reactive). 4 +__ ОН CH3 3. OH. Br 5 OH CH3 - 1 ОН NO2 - 2 ОН NO2
Arrange the following compounds in increasing order of their reactivity to electrophiles. (least reactive first) A. CH CHO (benzaldehyde) B. C&HOCH, (anisole) C. C HBr (bromobenzene) D. CH3CH, (toluene) 1) A<C<D<B 2) A<D<C< B 3 ) C<A<B<D 4) C<A<D<B Nitration of chlorobenzene occurs: 1) faster than nitration of benzene and gives the ortho and para products. 2) faster than nitration of benzene and gives the meta product. 3) slower than nitration of benzene and gives the ortho and para products....
,,,,,,,,,,,
Rank the compounds below in order of decreasing reactivity towards electrophilic aromatic substitution. Most reactive Least reactive COOH H3C CH3 COOH HaC
Rank the compounds below in order of decreasing reactivity towards electrophilic aromatic substitution Most reactive Least reactive COOH H3C CH3 HOOC- COOH
Rank the following isomers in order of increasing heat of formation. Incorrect. The aromatic compound is the most stable in this group, so it has the lowest heat of formation.