Homework Answers
29. Option C, regiochemistry which means that at which position reaction occurs to a particular group. EWGs gives meta reaction on benzene ring while EDGs gives o/p reactions.
30. Option E, Friedal-Crafts acylation/Alkylation. Especially AlCl3 is used as Lewis acid.
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29. A blocking group can be used to control the outcome of an EAS? A) yield...
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...
10) 10) When the carbonyl group of a ketone is protonated A) the resulting species is...
10) 10) When the carbonyl group of a ketone is protonated A) the resulting species is activated toward nucleophilic addition B) the resulting species becomes more electrophilic subsequent nucleophilic addition on the resulting species is said to occur under acid-catalyzed conditions D) the resulting species has a positive charge. E) all of the above 11) What purpose does FeCl3 serve when benzene undergoes an electrophilic aromatic substitution reaction with chlorine? A) It serves as a Lewis base catalyst by reacting...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
The following is an example of an O-linked oligosaccharide chain in oligosaccharide is linked to the protein by the side-chain functional B the side-chain functional group of serine or thre...
The following is an example of an O-linked oligosaccharide chain in oligosaccharide is linked to the protein by the side-chain functional B the side-chain functional group of serine or threonine residues. Fuda2-12) Gal(β1-34)GlcNAc(B1-4) aride chain in glycoproteins. The O-linkage means the GlcNAc(a1 )-) Serine GalNAc(al>3) al(B1- 4)GIcNAc(B13) Gal(B1->4)GIcNAc(3)G1>3) Fuc(a22) Draw out this polymer from the following Fischer projections of the monosaccharide. 1) Show each monosaccharide in the Haworth projection and in the Chair conformation for the six-member rings. 2) Show...
NAME! Select the best answer and bubble it in on your blue scantron. 1. Where would...
NAME! Select the best answer and bubble it in on your blue scantron. 1. Where would be the absorption peak of a carbonyl, C-0, stretching in IR? a) around 3300 cm b) around 2980 cm" c) around 1700 cm d) around 1200 cm 2. What is the Grignard reagent in nucleophilic addition reaction considered? a) b) 0 c) H d) all the above 3. What a cynaohydrin contains? a) CN and NH. b) N, and OH. c) CN and OH....
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,...
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...
10) 10) When the carbonyl group of a ketone is protonated A) the resulting species is activated toward nucleophilic addition B) the resulting species becomes more electrophilic subsequent nucleophilic addition on the resulting species is said to occur under acid-catalyzed conditions D) the resulting species has a positive charge. E) all of the above 11) What purpose does FeCl3 serve when benzene undergoes an electrophilic aromatic substitution reaction with chlorine? A) It serves as a Lewis base catalyst by reacting...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
The following is an example of an O-linked oligosaccharide chain in oligosaccharide is linked to the protein by the side-chain functional B the side-chain functional group of serine or threonine residues. Fuda2-12) Gal(β1-34)GlcNAc(B1-4) aride chain in glycoproteins. The O-linkage means the GlcNAc(a1 )-) Serine GalNAc(al>3) al(B1- 4)GIcNAc(B13) Gal(B1->4)GIcNAc(3)G1>3) Fuc(a22) Draw out this polymer from the following Fischer projections of the monosaccharide. 1) Show each monosaccharide in the Haworth projection and in the Chair conformation for the six-member rings. 2) Show...
NAME! Select the best answer and bubble it in on your blue scantron. 1. Where would be the absorption peak of a carbonyl, C-0, stretching in IR? a) around 3300 cm b) around 2980 cm" c) around 1700 cm d) around 1200 cm 2. What is the Grignard reagent in nucleophilic addition reaction considered? a) b) 0 c) H d) all the above 3. What a cynaohydrin contains? a) CN and NH. b) N, and OH. c) CN and OH....
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,...
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