Nil 1. Which of the following compounds is least reactive by electrophilic aromatic nitration or sulfonation?...
1. Which compound is the least reactive in the aromatic electrophilic substitution reaction? A NH B. NH C. SOH D. NOZ E. Seunal volo montubong tomorú od
Which compound is the least reactive in the aromatic electrophilic substitution reaction? What product would you expect from the following reaction? Answer both, please. 1. Which compound is the least reactive in the aromatic electrophilic substitution reaction? NH . B NH С. SOH Logo D. NO2 E 2. What product would you expect from the following reaction? CO.CH ÇO.CH А ÇOCH B OCH, D CO.CH E
please help in all sections asap!! Which of the following reactions would produce isopropylbenzene as the major product? ОН AICI: H2SO4 H2SO4 AICI3 IV I all of these Predict the product for the following reaction fuming H2SO4 SO3H Predict the structure of the major product for the following reaction Which of the following compounds will not undergo nucleophilic aromatic substitution? 1-chloro-2,4-dinitrobenzene 1-bromo-4-nitrobenzene O-chloronitrobenzene m-chloronitrobenzene p-chloronitrobenzene Choose the correct sequence of reagents for the following transformation. 2) 3 . NH2 2)...
Rank the compounds below in order of decreasing reactivity towards electrophilic aromatic substitution Most reactive Least reactive COOH H3C CH3 HOOC- COOH
please help in all sections asap!! Provide the reagents necessary to carry out the following conversion. CCH3 Choose the correct reagents for step 1. CH3CH2Cl / AICI Cl2 / AICI Bry/ FeBry CH3CCI / AICI: Choose the correct reagents for step 2. NON CH3CH2C / AICI Cl2 / AICI Bry/FeBry o CH,CCI/ AICI Predict the major product for the following reaction. CI/AICI: ОН ОН ОН 0 none of these Provide the reagents necessary to carry out the following conversion. Choose...
Which of the following compounds is the most reactive toward electrophilic aromatic substitution? IV H III IT IN
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....
1,3–Dimethoxybenzene (below) is very reactive toward electrophilic aromatic substitution. Draw a complete mechanism for the following nitration reaction making sure you include details of formation of the required electrophile and all possible delocalized structures for the intermediate cation. Provide a brief explanation for why only the pictured product is formed:
Please help with these practices. Which undergoes the fastest electrophilic substitution with Br2 or AlBr3? Which substrate undergoes the most rapid electrophilic substitution with HNO3/H2SO4? Which reaction sequence results in this? What is the major product for the reaction? CH3 Оснз осна осна Br Б) с) d) NO2 осна осна OCH2CH3 OCH2CH3 H2C a) b) c) d) CH3 SO3H NO2 SO3H OCH3 Br OCH3 CI a) SO3 H2SO4 HNO3 H2SO4 Pd(OAC)2 AICI: (HO)2B OCH3 Br2 b) HNO3 H2SO4 SO3 H2SO4...
Write complete equations (using structures) to the following sequence of reactions and give the structures of compounds A through I. Neatness counts B AICI, HNO H2SO4 Zn(Hg) HCI KMnO с (hot, coned.) D NH BIZ NH, hv (CH3),COK E Heat NaOCH Cyclopentadiene/Heat G H F