The correct option is, a deactivator and an o,p- director.
Like halides, nitroso group is an Ortho , para directing but acts as deactivator.
2. In electrophilic aromatic substitution reactions, a substituent (i.e., nitroso group) on the aromatic ring is:...
1. In electrophilic aromatic substitution reactions a bromine substituent: A) is a deactivator and a m-director. C) is an activator and a m-director. E) none of the above B) is a deactivator and an o,p-director. D) is an activator and an o,p-director. 2. Provide a detailed, stepwise mechanism for the reaction of benzene with Br2 and FeBr3. Make sure to include the activating reaction between Br2 and FeBr3 in your mechanism.
Predict the effect the substituent attached to the benzene ring below would have on electrophilic aromatic substitution reactions? CH, CH3 a) meta director, deactivator b) ortho/para director, activator c) meta director, activator d) ortho/para director, deactivator
a. Is the -NO2 group an activator or a deactivator with respect to electrophilic 2. aromatic substitution reactions? b. Does the -NO2 group direct a second substituent ortho, meta or para? Is the -NO2 group an activator or a deactivator with respect to nucleophilic 3. aromatic substitution reactions?
1) Which of the following is an intermediate in the bromination of toluene? p) Ha BrH 2 2) Under what reaction conditions would the electrophilic chlorination of aromatic compounds usually occur? A) Cl2, AlCl3 B) C12, CCl4 C) Cl2, H20 D) NaCl, H20 E) NaCI, CH3OH 3) 3) Which of the following is the strongest activating group in electrophilic aromatic substitution reactions? A) -CO2CH3 B)-NO2 C) -OCH3 D) -CH2CH3 E) -N(CH3)2 4) _ 4) In electrophilic aromatic substitution reactions the...
9:09 AM Mon Apr 29 ゃしダ46% ■ f) What is the major organic product obtained from the following reaction? CrOs он HSO,, H20 1-butene, CH,CH,CH CH butanal, CH CH.CH,CHO CH,CH,COCH butanoic acid, CH,CH,CH,COO g) In electrophilic aromatic substitution reactions a bromine substituent A) is a deactivator and a m-director. B) is a deactivator and an o,p-director. C) is an activator and a m-director D) is an activator and an o,p-director E) none of the above h) In electrophilic aromatic substitution...
1) What is/are the product (s) in the following reaction so,0, A) I only B) Il only C) III only D) II and IV E) I and IV 2) A -NO2 substituent on the aromatic ring is a _in electrophilic aromatic substitution reactions. A) a deactivator and a m-director. B) a deactivator and an o,p-director. C) an activator and a m-director. D) an activator and an o,p-director. 3) Which compound would be expected to show a broad peak around 3000cm-1?...
Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution reactions. Substituents can activate or deactivate the ring to substitution, donate or withdraw electrons inductively, donate or withdraw electrons through resonance, and direct substitution either to the ortho/para or to the meta positions. From the following lists, select the substituents that have the indicated property. The substituents are written as -XY, where X is the atom directly bound to the aromatic ring. Substituents on an aromatic ring...
Substituents on an aromatic ring can have several effects on electrophilic aromatic substitution reactions. Substituents can activate or deactivate the ring to substitution donate or withdraw electrons through resonance, and direct substitution either to the ortho/para or to the meta positions. From the following lists, select the substituents that have the indicated property. The substituents are written as -XY, where X is the atom directly bound to the aromatic ring. Activation of the ring towards substitution. Withdrawal of electrons through...
4. Answer the following questions based on the electrophilic aromatic substitution reaction shown below. door a. (2.5pts) Based on the identity of the substituent on the starting material and its interaction with the aromatic ring, is this substituent an activator or deactivator? Briefly explain your answer and support your answer with structures b. (5.5pts) Draw all of the resonance contributors of the o-complexes that lead to each of the three possible products. c. (0.5p) Based on the structures drawn in...
(6 pts) The -NH2 group is listed in our textbook as the strongest activator in electrophilic aromatic substitution reactions. However, -NHCOCH3 is listed as a moderate activator and -cONH2 is listed as a moderate deactivator. Using resonance structures show why this statement is correct.