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OH is good activating group and amide is deactivated group. Hence Substitution occurs at para to OH and meta to amide.
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Salicylamide is another active pharmaceutical ingredient that is commonly used for pain relief. A...
Please help with questions 1-5. I have attached the additional lab information pages for help if...
Please help with questions 1-5. I have attached the additional
lab information pages for help if you are unclear on anything
please review those.
We were unable to transcribe this imageEAS 97 5. Calculate the theoretical yiel te the theoretical yield of iodinated salicylamide (product) ass Todination reaction. (Show your calculations.) mide (product) assuming a mono- le, your starting material, is shown in Figure 4. ces in the functional group region of the spectrum IR spectrum of salicylamide, your starting...
Why is sodium thiosulfate used in this experiment? slow fa st + H-Y H aromaticity destroyed...
Why is sodium thiosulfate used in this experiment?
slow fa st + H-Y H aromaticity destroyed H aromaticity restore A variety of electrophiles (Ey will react with benzene, and derivatives of benzene, to yield substitution products. Halogenation of benzene rings is an important reaction Br Pentab PBDE Br have important uses, e.g, pentabromodiphenyl ether CH PBDE; flame retardant) and Vancomycin (naturally because H, occurring antibiotic). However, halogens are not very CH, reactive toward benzene rings. and for this reason, they...
use the notes provided to help answer the question above. will rate well The second step...
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....
Please help with questions 1-5. I have attached the additional
lab information pages for help if you are unclear on anything
please review those.
We were unable to transcribe this imageEAS 97 5. Calculate the theoretical yiel te the theoretical yield of iodinated salicylamide (product) ass Todination reaction. (Show your calculations.) mide (product) assuming a mono- le, your starting material, is shown in Figure 4. ces in the functional group region of the spectrum IR spectrum of salicylamide, your starting...
Why is sodium thiosulfate used in this experiment?
slow fa st + H-Y H aromaticity destroyed H aromaticity restore A variety of electrophiles (Ey will react with benzene, and derivatives of benzene, to yield substitution products. Halogenation of benzene rings is an important reaction Br Pentab PBDE Br have important uses, e.g, pentabromodiphenyl ether CH PBDE; flame retardant) and Vancomycin (naturally because H, occurring antibiotic). However, halogens are not very CH, reactive toward benzene rings. and for this reason, they...
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....
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