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Friedel-Crafts acylation followed by reduction is a convenient way to synthesize straight-chain alkylbenzenes. Why does the...
Benzene underwent a Friedel-Crafts acylation reaction followed by a Clemmensen reduction. The product gave the 1H...
Benzene underwent a Friedel-Crafts acylation reaction followed
by a Clemmensen reduction. The product gave the 1H NMR
spectrum shown above. What acyl chloride was used in the
Friedel-Crafts acylation reaction? Hint: It would be helpful
if you first assign a structure to the compound shown in the
1H NMR spectrum.
Benzene underwent a Friedel-Crafts acylation reaction followed by a Clemmensen reduction. The product gave the 1H NMR spectrum shown above. What acyl chloride was used in the Friedel-Crafts acylation reaction?...
The following questions are from an experiment titled Friedel-Crafts Alkylation for Organic Chemistry II Lab. There...
The following questions are from an experiment titled
Friedel-Crafts Alkylation for Organic Chemistry II Lab. There are
pictures attached of the lab manual.
2) Is this method a good route for the preparation of
p-sec-butyltoulene? Give reasons for your answer.
3) Why do you use a large excess of toulene. What are its
functions?
4) What is the purpose for adding the hydrochloric acid to the
water in the separatory funnel in step 5? Hint: If no acid is
added,...
1.Friedel-Crafts acylation of ortho-nitrotoluene with acetyl chloride and aluminum trichloride gives: A.a mixture of acetophenones with...
1.Friedel-Crafts acylation of ortho-nitrotoluene with acetyl chloride and aluminum trichloride gives: A.a mixture of acetophenones with the nitro group always ortho or para to the carbonyl. B.almost exclusively a single product, 3-nitro-4-methyl-acetophenone. C.2-methyl-acetophenone by nitro group displacement. D.no reaction since the nitro group is so deactivating. 2.You decide to make meta-nitrophenol by doing which of the following steps? A.Reacting phenol with fuming nitric acid in an ice bath. B.Reacting benzene with fuming nitric acid, then reacting the product with chlorine/iron,...
Chern 204-PSI, 6 . Friedel Crafts Acylation of an Unknown Benzene Compound (One weck lab The...
Chern 204-PSI, 6 . Friedel Crafts Acylation of an Unknown Benzene Compound (One weck lab The Intent of this Lab To acetylate an unknown benzene compound via a Friedel-Crafts acylation and use spectroscopic techniques to determine the acetophenone derivative's identity Introduction The Friedel-Crafts reaction dates back to before 1900 and it is still widely used today. The active electrophilic agent (an acylium ion) is classically prepared and reacts very quickly. Another appealing feature of this reaction is that the acylated...
Benzene underwent a Friedel-Crafts acylation reaction followed
by a Clemmensen reduction. The product gave the 1H NMR
spectrum shown above. What acyl chloride was used in the
Friedel-Crafts acylation reaction? Hint: It would be helpful
if you first assign a structure to the compound shown in the
1H NMR spectrum.
Benzene underwent a Friedel-Crafts acylation reaction followed by a Clemmensen reduction. The product gave the 1H NMR spectrum shown above. What acyl chloride was used in the Friedel-Crafts acylation reaction?...
The following questions are from an experiment titled
Friedel-Crafts Alkylation for Organic Chemistry II Lab. There are
pictures attached of the lab manual.
2) Is this method a good route for the preparation of
p-sec-butyltoulene? Give reasons for your answer.
3) Why do you use a large excess of toulene. What are its
functions?
4) What is the purpose for adding the hydrochloric acid to the
water in the separatory funnel in step 5? Hint: If no acid is
added,...
Chern 204-PSI, 6 . Friedel Crafts Acylation of an Unknown Benzene Compound (One weck lab The Intent of this Lab To acetylate an unknown benzene compound via a Friedel-Crafts acylation and use spectroscopic techniques to determine the acetophenone derivative's identity Introduction The Friedel-Crafts reaction dates back to before 1900 and it is still widely used today. The active electrophilic agent (an acylium ion) is classically prepared and reacts very quickly. Another appealing feature of this reaction is that the acylated...
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