r each compound below, identify which position(s) is/are most likely to undergo an electrophilic aromatic substitut...
!!! If each compound undergoes electrophilic aromatic substitution, where should the substituent be added? *The choices for each are either ortho/para position OR meta position.* Phenol? Benzaldehyde? Benzoic Acid? Bromobenzene? Nitrobenzene? Toluene?
4) Rank the compounds in each group according to their reactivity toward electrophilic aromatic substitution a) Benzene, benzenesulfonic acid, o-dibromobenzene a) p-Bromotoluene, nitrobenzene, aniline a) o-Xylene, phenol, benzaldehyde
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.
Practice the Skill 18.18 For each compound below, identify which position(s) is/are most likely to undergo an electrophilic aromatic substitution reaction based on electronic effects only. x Your answer is incorrect. Try again. x Your answer is incorrect. Try again. meton
(Review Topics] (References) In both series below the three aromatic compounds illustrated undergo the electrophilic substitution reaction shown CH3 CH3 NO2 NO2 NO2 , Reaction: Nitration Which compound (A, B, or C) reacts the fastest? - Which compound (A, B, or C) reacts the slowest? - D D OCHZ COH Reaction: Chlorination Which compound (A, B, or C) reacts the fastest? Which compound (A, B, or C) reacts the slowest? _D
TRUVIOw Topics (References] In both series below the three aromatic compounds illustrated undergo the electrophilic substitution reaction shown O=0 C- H CH2CH2CH2CH3 Reaction: Chlorination Which compound (A, B, or C) reacts the fastest? Which compound (A, B, or C) reacts the slowest? _ OCH3 OCH3 NO2 NO2 Reaction: Nitration Which compound (A, B, or C) reacts the fastest? – Which compound (A, B, or C) reacts the slowest? –
ch 22 In both series below the three aromatic compounds illustrated undergo the electrophilic substitution reaction shown NH2 A B Reaction: Bromination Which compound (A, B, or C) reacts the fastest? Which compound (A, B, or C) reacts the slowest А B с Reaction: Chlorination Next Reaction: Bromination Which compound (A, B, or C) reacts the fastest? Which compound (A, B, or C) reacts the slowest? v do 000!! ZI Reaction: Chlorination Which compound (A, B, or C) reacts the...
h both series below the three aromatic compounds ilhestrated undergo the electrophilic substitution reaction show NHCCHE A B Reaction: Bromination Which compound (A, B, C) reacts the fastest? Which compound (A, B, or C) reacts the slowest? O OCH COH A B C Reaction: Chlorination Which compound (A, B, or C) reacts the fastest? Which compound (A, B, or C) reacts the slowest? h both series below the three stomatic compounds ilhestrated undergo the electrophilic substitution reaction shown -C-CH2CH3 OH...
Edit Vow History Bookmarks Window Heip 100% " Sun 726 PM Heterocyclic aromatic compounds undergo electrophilic anomatic substitution in a similar fashion to that undergome by benzene with the formation of a Draw all of the resonance contributoes expected when the above compound undergoes bromination at position 2 De non inchade lone pairs in your answer. They will sot be considesed in the grading * Daw ore structue per skewher Add adhoonal sketchers using the dropdown鬧u in the bottom nght...
Help!!!!!! Aromatic Nitration QUESTIONS 1 Which compound in each of the following pairs is more reactive towards aromatic nitration? Expl your answers. a. phenol or nitrobenzene b. methyl benzoate or phenol c. nitrobenzene or methyl benzoate d. benzene or toluene 2. Show all possible mononitration products of toluene. Do you think it would be easy to isolate and identify all of them if each is produced in some amount? PRELABORATORY QUESTIONS 1. Lis three different combinations of reagents used for...