Homework Answers
The reactions are given as follows,
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14) Provide the correct products obtained with acetophenone reacts under each of the following conditions. acetophenone...
provide the reaction conditions and the structure of the correct products of the following reaction Provide...
provide the reaction conditions and the structure of the
correct products of the following reaction
Provide the reaction conditions and the structure of the correct products of the following reactions: H.CH, OH heat .heat HO ΝΗ,
Provide the structures of the expected products when 1-pentyne reacts under the following conditions. Note: Diisoamylborane...
Provide the structures of the expected products when 1-pentyne
reacts under the following conditions. Note: Diisoamylborane is a
reagent which reacts just like borane.
3. Provide a complete curved-arrow mechanism for each of the following transformations OH 에 HAOLO 1....
3. Provide a complete curved-arrow mechanism for each of the following transformations OH 에 HAOLO 1. NaOH cat 2. NaBH, MOH - HO HOON N (Hint: recall from lecture that sugars like this often exist as hemiacetals!) no HO CN NaCN, ETOH 80 °C T
IVA. Predict the organic products formed in each of the following reactions of acetophenone. (12 points)...
IVA. Predict the organic products formed in each of the following reactions of acetophenone. (12 points) .H,O 1. PhMgBr, Et, 2. H2O 1. NaBH, CH,OH 2. H,O* 2 CH,CH,OH, H,00 IVB. Show a detailed mechanism (using curved arrows) for the Grignard reaction in question IVA between acetophenone and phenyl magnesium bromide (6 points)
Provide the reaction conditions and the structure of the correct products of the following reactions: B...
Provide the reaction conditions and the structure of the correct products of the following reactions: B HO CH₃OH heat А Ho neat -H₂O С. hata show stepwise how would you prepare the following compounds from the Provided starting material and other organic or morganic compound. OH i loc ANA starting materiale А HO ii Oct OEt B starting material
pppppplllleeeaaassseee help 1. a. Compound 1 reacts with A under acid conditions to form an imine. What could Z be in this reaction? b. Compound 2 reacts with A (same A as previous reaction) unde...
pppppplllleeeaaassseee help
1. a. Compound 1 reacts with A under acid conditions to form an imine. What could Z be in this reaction? b. Compound 2 reacts with A (same A as previous reaction) under acid conditions to form an amide. What is Z in this reaction? Draw the structure of A Use curved arrows to show how Compound 2 forms the amide. c. Both reactions involve a leaving group. What is the leaving group in each reaction? O A...
sodium borohydide reduction of 4 tert butylcyclohexanone. need help confirming top answers are correct and help...
sodium borohydide reduction of 4 tert
butylcyclohexanone. need help confirming top answers are correct
and help with lower section. thanks
& Draw your two products (each in the most stable chair conformation) below using the numbering provided. Show only the -OH and tert-butyl groups on the ring. a) label each group as equatorial (eq) or axial (ax). b) label each group as top face (top) or bottom face (bot). OH (ax, top) (ax, bot) .OH (Eq, top 7 (Er, top...
21 points provide reactants , products or conditions for the following single step reactions as indicated...
21 points provide reactants , products or conditions for the
following single step reactions as indicated
(21 points) Provide reactants, products or conditions for the following single step reactions as indicated. (put your answer in the box provided) Hg(OAc), CI Br + 0 HH NaBH, CH,CI, кон ETOH Brz water 1.03 2. Zn/acid 1. Oso 2. NaHSO3
1. Provide the missing starting materials, reagents, or products in each of the following reactions. H+...
1. Provide the missing starting materials, reagents, or products in each of the following reactions. H+ OH CH,OH NaOH Meo NH2 room temp. HO OH Meo Me ОН Meo 2. Provide appropriate conditions to convert each of the following starting mana hexanoic acid (some transformations may require more than one step): It each of the following starting materials into OH OH ОMe "NH₂
2) Provide a product for each of the following reactions. Ensure correct chemoselectivity, stereoselectivity and regioselectivity...
2) Provide a product for each of the following reactions. Ensure correct chemoselectivity, stereoselectivity and regioselectivity in product determination. OH SOCI (2eq) b) 1.0 2) H2O, NaOH - KMnO., NaOH, H2O H3C 1) Mg 2) CO. 3) H30 ОН Na Cr.O H2SO4, H,0 (excess) NaBH EtOH Hint: esterification H+ DLDA 2) PhCH,Br /4 736
provide the reaction conditions and the structure of the
correct products of the following reaction
Provide the reaction conditions and the structure of the correct products of the following reactions: H.CH, OH heat .heat HO ΝΗ,
Provide the structures of the expected products when 1-pentyne
reacts under the following conditions. Note: Diisoamylborane is a
reagent which reacts just like borane.
3. Provide a complete curved-arrow mechanism for each of the following transformations OH 에 HAOLO 1. NaOH cat 2. NaBH, MOH - HO HOON N (Hint: recall from lecture that sugars like this often exist as hemiacetals!) no HO CN NaCN, ETOH 80 °C T
IVA. Predict the organic products formed in each of the following reactions of acetophenone. (12 points) .H,O 1. PhMgBr, Et, 2. H2O 1. NaBH, CH,OH 2. H,O* 2 CH,CH,OH, H,00 IVB. Show a detailed mechanism (using curved arrows) for the Grignard reaction in question IVA between acetophenone and phenyl magnesium bromide (6 points)
Provide the reaction conditions and the structure of the correct products of the following reactions: B HO CH₃OH heat А Ho neat -H₂O С. hata show stepwise how would you prepare the following compounds from the Provided starting material and other organic or morganic compound. OH i loc ANA starting materiale А HO ii Oct OEt B starting material
pppppplllleeeaaassseee help
1. a. Compound 1 reacts with A under acid conditions to form an imine. What could Z be in this reaction? b. Compound 2 reacts with A (same A as previous reaction) under acid conditions to form an amide. What is Z in this reaction? Draw the structure of A Use curved arrows to show how Compound 2 forms the amide. c. Both reactions involve a leaving group. What is the leaving group in each reaction? O A...
sodium borohydide reduction of 4 tert
butylcyclohexanone. need help confirming top answers are correct
and help with lower section. thanks
& Draw your two products (each in the most stable chair conformation) below using the numbering provided. Show only the -OH and tert-butyl groups on the ring. a) label each group as equatorial (eq) or axial (ax). b) label each group as top face (top) or bottom face (bot). OH (ax, top) (ax, bot) .OH (Eq, top 7 (Er, top...
21 points provide reactants , products or conditions for the
following single step reactions as indicated
(21 points) Provide reactants, products or conditions for the following single step reactions as indicated. (put your answer in the box provided) Hg(OAc), CI Br + 0 HH NaBH, CH,CI, кон ETOH Brz water 1.03 2. Zn/acid 1. Oso 2. NaHSO3
1. Provide the missing starting materials, reagents, or products in each of the following reactions. H+ OH CH,OH NaOH Meo NH2 room temp. HO OH Meo Me ОН Meo 2. Provide appropriate conditions to convert each of the following starting mana hexanoic acid (some transformations may require more than one step): It each of the following starting materials into OH OH ОMe "NH₂
2) Provide a product for each of the following reactions. Ensure correct chemoselectivity, stereoselectivity and regioselectivity in product determination. OH SOCI (2eq) b) 1.0 2) H2O, NaOH - KMnO., NaOH, H2O H3C 1) Mg 2) CO. 3) H30 ОН Na Cr.O H2SO4, H,0 (excess) NaBH EtOH Hint: esterification H+ DLDA 2) PhCH,Br /4 736
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