consider the resonance structures of acetanilide and methylbenzoate provided above... Several resonance structures of acetanilide are...
Consider the resonance structures of acetanilide and methylbenzoate provided above. a. How does the-COOCH3 substituent on methylbenzoate direct? b. Do the partial charges shown on either acetanilide or methyl-benzoate activate or deactivate the electrophilic substitution reaction? C. Is there a correlation between directing and activating groups? Explain.
Consider the resonance structures of acetanilide and methyl benzoate provided above. How does the -COOCH3 substituent on methyl benzoate direct? Do the partial charges shown on either acetanilide or methyl-benzoate activate or deactivate the electrophilic substitution reaction? Is there a correlation between directing and activating groups? Explain. I Resonance structures of methyl-benzoate and the resulting partial charges are shown below. How does the benzoate group direct? 0: -1 =O :00 00 OA Several resonance structures of acetanilide are shown below:...
Please help... Need a detail Mechanism of this reaction. Thanks... Electrophilic aromatic substitution describes the reaction where a hydrogen from a benzene ring is replaced by an electrophile. Halogenation, nitration, sulfonation, alkylation and acylation are all possible using this type of reaction. The electrophile attacks the pi electrons of the aromatic ring, yielding a benzenonium ion. The substituted aromatic product is obtained when a proton is lost, restoring the aromatic system. If there is a substituent on the aromatic ring...
Four major resonance structures are possible for the following cation, the sigma complex of an electrophilic aromatic substitution. Three are given below, but are incomplete. Complete the given structures by adding nonbonding electrons and formal charges. Draw the remaining structure, including nonbonding electrons and formal charges.
........... our major resonance structures are possible for the following cation, the o Complex of an electrophilic Map aromatic substitution. Three are given below, but are incomplete. Complete the given structures by addirrg nonbonding electrons and formal charges. Draw the remaining structure, including nonbonding electrons and formal charges Br (Scroll down)
Four major resonance structures are possible for the following cation, the complex of an electrophilic aromatic substitution. Three are given below, but are incomplete. Complete the given structures by adding nonbonding electrons and formal charges. Draw the remaining structure, including nonbonding electrons and formal charges. (Scroll Previous Check Answer Next
Friedel - Craft Acylation Synthesis of 4-Methoxiacetophenone Background Information 1.- What is an electrophilic aromatic substitution? 2.- Give three examples of activating groups. Explain why they activate the ring for substitution. 3.- Give three examples of deactivating groups. Explain why they deactivate the ring for substitution. 4.- Describe the difference between a Friedel-Craft alkylation and Acylation. Synthesis of 4-Methoxiacetophenone For this Friedel-Craft acylation we will react Anisole with Acetic Anhydride. Write the mechanism and the structure of the final product....
Add the following questions to the final report: a) Why does the carbomethoxy group directs the reaction to positions that are meta to it? b) Why the formation of dinitrobenzaote is substantially disfavored ? c) Would you expect small amounts of the ortho and para substituted product? How would you remove them if they are formed ? d) Why does water have a retarding effect on the nitration ? e) Explain why Benzene has lower reactivity in electrophilic addition reactions...
use the notes provided to help answer the question above. will rate well The second step of the synthesis transformation of the chlorosulfonyl functional group into a sulfonamide) is an example of a a. Nucleophilic displacement (substitution) b Elimination C. Electrophilic aromatic substitution d. Acid hydrolysis Esterification e. THE SULFONIC ACID GROUP AND ITS DERIVATIVES Sulfonic acids are organic analogs of sulfuric acid, a very strong acid. They are highly corrosive, react vigorously with water, and can cause skin bums....
The rate constants for the bromination of several disubstituted stilbenes are given in the table below Given that the double bond of stilbene acts as the nucleophile, choose the reasonable explanations for the trend observed among the rate constants. Select all that apply. The nitro group is powerfully electron-withdrawing, via resonance which will reduce the nucleophilicity of the alkene pi bond. Methoxy group is a powerful activator, so its effect should be larger than the effect of a methyl group...