Consider the reactivity of phenol, bromobenzene, toluene, and nitrobenzene toward electrophilic aromatic substitution.
1.) The most reactive compound is (pick one: phenol, bromobenzene, toluene, and nitrobenzene) because the (pick one: electron donating or electron withdrawing) character of the (pick one: alcohol group, methyl group, bromine atom, or nitro group) increases the rate of the reaction.
2.) The least reactive compound is (pick one: phenol, bromobenzene, toluene, and nitrobenzene) because the (pick one: electron donating or electron withdrawing) character of the (pick one: alcohol group, methyl group, bromine atom, or nitro group) decreases the rate of the reaction.
Consider the reactivity of phenol, bromobenzene, toluene, and nitrobenzene toward electrophilic aromatic substitution. 1.) The most...
the options in the drop down boxes are phenol, bromobenzene, toluene, nitrobenezene Consider the reactivity of phenol, bromobenzene, toluene, and nitrobenzene toward electrophilic aromatic substitution. The most reactive compound is Choose... because the Choose... character of the Choose... increases the rate of the reaction. The least reactive compound is Choose... because the Choose... character of the Choose... decreases the rate of the reaction.
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
!!! 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?
rank the following compounds on the basis of reactivity toward electrophilic aromatic substitution use 1 for most reactive and 4 for least Provide the major enolRank the following compounds on the basis of reactivity toward electrophilic aromatic substitution use 1 for most reactive and 4 for least
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.
Question 2 0.5 pts Rank each group of aromatic compounds according to their reactivity toward electrophilic substitution: a. Benzonitrile, p-methylbenzonitrile, p-methoxybenzonitrile b. Fluorobenzene, benzaldehyde, o-xylene c. Phenol, nitrobenzene, p-cyanonitrobenzene
List of the following compound according to their reactivity towards electrophilic substitution. 072) List the following compound according to their reactivity towards electrophilic sust. 10-dibromienzene, benzene, bromobenzene (3 marks) () pamethylbenzonitrile, p-methoxybenzonitrile, benzonitrile (3 marks) (ii) Flamwobenzene, benzaldehyde, o-xylene auss on the substituent effect on aromatic reaction (3 marks) ny alkylation of nitro benzene will not occur (6 marks) (5 marks) Page 2 of 5
Which of the following statements is (are) true about electrophilic aromatic substitution? A. OCH, is an o, p activator because of a strong electron donating resonance effect. B. OCH, is an o, p director because of a strong electron withdrawing inductive effect. C. OCH, is an o, p activator because the O atom is an electronegative atom. D. Both statements (OCH, is an o, p activator because of a strong electron donating resonance effect) and (OCH, is an o, activator...
1. please check what is wrong. Thank you! Determine the product formed when each compound is treated with Br2 and FeBr3. Drag the atom labels to their appropriate positions. CN Atom labels H H Br Br2 A. FeBr Br H OH OH Br Br. Br2 FeBr3 H H Br Br H Br2 FeBr H1 H Reset T Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic substitution. CI Decreasing reactivity Rank the compounds in each...
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...