Homework Answers
![и би М] л. , е от еды , а 1 on NOBH, doesno reduces c=cand ester carbonyl group It only reduces a keterse group.](http://img.homeworklib.com/questions/330c3210-d772-11eb-b1ff-67fb162c72c1.png?x-oss-process=image/resize,w_560)
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4. Provide reasonable products or reactants for the reactions below. (a) (reaction of aldehyde/ketone) H' Η...
4. Fill-in-the-blanks: draw the missing reactants or products involved in the following single or multi-step reactions....
4. Fill-in-the-blanks: draw the missing reactants or products involved in the following single or multi-step reactions. Indicate stereochemistry and draw multiple stereoisomers where applicable. i EtOH EtOH [H2SO4] 1) EtMgBr 2) H20 5. For most ketones, hydrate formation is unfavorable, because the equilibrium favors the ketone rather than the hydrate. However, the equilibrium for hydration of hexafluoroacetone favors the hydrate. Propose a mechanism for this transformation below and provide an explanation for this observation. H2O Но он F3CX CF3 F3C...
wone br Provide the products of the following reaction scheme. 5' x 9 45 1)O 2)...
wone br Provide the products of the following reaction scheme. 5' x 9 45 1)O 2) DIAS 1) OsO 2) NAHSO но нх HDr лOOR но 1) RCO H 2) но 1) Hg(OAc) HO NabH "он Big H,O 1) вн, тHP 2) HO NaoH 7 6 5
1. What will be the products (A-D) in the following aldehyde and ketone reactions ? Hoon...
1. What will be the products (A-D) in the following aldehyde and ketone reactions ? Hoon 1) SOCI 2) (CH3)2NH A FO сндон, H30* OH B CH H₃C. OH H3C Pyridine H3C CH, с مل CH3NH2, A D 2. Provide IUPAC names for the following compounds (E-G). Name: нас. сн, сн. E Name: H3C CH3 CH3 F Name: HO OH CH3 G 3. Provide a mechanism for the following reactions a) OCH3 CH3NH2, 4 NHCH3 b) FO 1) SOCI 2)...
Please help with both if possible! 1. Provide the missing reactants or products for the reactions...
Please help with both if possible!
1. Provide the missing reactants or products for the reactions shown below. Provide the structure(s) in the boxes provided. (8 points) a. Na o= 1. CH3Mgi 2. H30 2. H:0* 1. CH3Li 2. H30* 2. Provide the reaction mechanism for the reaction shown below. (4 points) cat. H ОН + H2O ОН
. 1) Draw ChemSketch or hand-drawn and name the posible aldehyde and ketone Isomers with CHO...
. 1) Draw ChemSketch or hand-drawn and name the posible aldehyde and ketone Isomers with CHO molecular formula 2 Based on your textbook, show the vidation reaction of each isomer. If there is no reaction, type R . for the following compounds 1. Provide molecular formula 2. Provide IUPAC 3. Show addition of hydrogen reaction draw structures of the products and provide IUPAC name for the products O a 0 1) Draw (ChemSketch or hand-drawn) and name all the possible...
Predict the products Predict the Product. Provide the stable organic product(s) for each reaction below NaBH...
Predict the products
Predict the Product. Provide the stable organic product(s) for each reaction below NaBH CHOH 1 2 HCI, H,0 NaBH, (1 вg.)., сн,он 1. 2. HC, н,о 1. NaBH(осH (1 eq.), сн,он CI 2. HCI, H,O 1. LIAIH (1 eq.), THF Br 2. HCI, H2O
1. (4 pts) Provide products for the following reactions indicated below: NEOEU: HCI d. Citymalanato NEOEI...
1. (4 pts) Provide products for the following reactions indicated below: NEOEU: HCI d. Citymalanato NEOEI il. HCL H-0 EIO OET + NaOH 100C Ph. i H H H HON NaBH CN O Br NH ј кон 2 HNNH, NH ex
plz help Which aldehyde or ketone AND amine reactants are needed to complete the following reaction?...
plz help
Which aldehyde or ketone AND amine reactants are needed to complete the following reaction? CEO NaBH,CN Amine dil. H30+ N(CH3)3 NH(CH3 N(CH3)3 Predict the product(s) for the following reaction series: ОН -Br 1) NaH 2) ОН + -ONa A decapeptide that is part of an insulin-like peptide has the molecular formula: Asn, Arg(2), Ser(3), Phe, Cys, Leu, Thr. After partial hydrolysis, the fragments are: Cys-Ser-Phe-Ser- Arg-Asn-Ser-Cys Thr-Leu-Arg Ser-Thr What is the sequence? Ser-Phe-Ser-Thr-Leu-Arg-Arg-Asn-Ser-Cys Ser-Thr-Arg-Asn-Ser-Cys-Ser-Phe-Ser- Asn Arg-Asn-Ser-Cys-Ser-Phe-Ser-Thr-Leu-Arg Thr-Leu-Arg-Asn-Ser-Cys-Ser-Phe-Ser-Phe
pts) Give the missing reagents, reactants or products in the following reactions: (each box or blank...
pts) Give the missing reagents, reactants or products in the following reactions: (each box or blank iš U. 1. give name only give name only SOCI2 H2CRO4 1. ВНз H, heat (Fischer Esterification) 2. H202, HO Он propene + AICI3 (F.C. acyla give structure and IUPAC name: Br2/FeBr3
3. Provide a full arrow-pushing mechanism for each of the following reactions. Но, он НО Но...
3. Provide a full arrow-pushing mechanism for each of the following reactions. Но, он НО Но он і - H- 0ң но он Насо, осна Нt H2O 4. A researcher wants to run the following sequence of reactions. However, they know starting Grignard reagent cannot exist due to the presence of its reactive carbonyl group. MgBr H.H cannot exist! An acetal group can be used to protect" a carbonyl from attack, allowing it to survive otherwise incompatible reaction conditions. Provide...
4. Fill-in-the-blanks: draw the missing reactants or products involved in the following single or multi-step reactions. Indicate stereochemistry and draw multiple stereoisomers where applicable. i EtOH EtOH [H2SO4] 1) EtMgBr 2) H20 5. For most ketones, hydrate formation is unfavorable, because the equilibrium favors the ketone rather than the hydrate. However, the equilibrium for hydration of hexafluoroacetone favors the hydrate. Propose a mechanism for this transformation below and provide an explanation for this observation. H2O Но он F3CX CF3 F3C...
wone br Provide the products of the following reaction scheme. 5' x 9 45 1)O 2) DIAS 1) OsO 2) NAHSO но нх HDr лOOR но 1) RCO H 2) но 1) Hg(OAc) HO NabH "он Big H,O 1) вн, тHP 2) HO NaoH 7 6 5
1. What will be the products (A-D) in the following aldehyde and ketone reactions ? Hoon 1) SOCI 2) (CH3)2NH A FO сндон, H30* OH B CH H₃C. OH H3C Pyridine H3C CH, с مل CH3NH2, A D 2. Provide IUPAC names for the following compounds (E-G). Name: нас. сн, сн. E Name: H3C CH3 CH3 F Name: HO OH CH3 G 3. Provide a mechanism for the following reactions a) OCH3 CH3NH2, 4 NHCH3 b) FO 1) SOCI 2)...
Please help with both if possible!
1. Provide the missing reactants or products for the reactions shown below. Provide the structure(s) in the boxes provided. (8 points) a. Na o= 1. CH3Mgi 2. H30 2. H:0* 1. CH3Li 2. H30* 2. Provide the reaction mechanism for the reaction shown below. (4 points) cat. H ОН + H2O ОН
. 1) Draw ChemSketch or hand-drawn and name the posible aldehyde and ketone Isomers with CHO molecular formula 2 Based on your textbook, show the vidation reaction of each isomer. If there is no reaction, type R . for the following compounds 1. Provide molecular formula 2. Provide IUPAC 3. Show addition of hydrogen reaction draw structures of the products and provide IUPAC name for the products O a 0 1) Draw (ChemSketch or hand-drawn) and name all the possible...
Predict the products
Predict the Product. Provide the stable organic product(s) for each reaction below NaBH CHOH 1 2 HCI, H,0 NaBH, (1 вg.)., сн,он 1. 2. HC, н,о 1. NaBH(осH (1 eq.), сн,он CI 2. HCI, H,O 1. LIAIH (1 eq.), THF Br 2. HCI, H2O
1. (4 pts) Provide products for the following reactions indicated below: NEOEU: HCI d. Citymalanato NEOEI il. HCL H-0 EIO OET + NaOH 100C Ph. i H H H HON NaBH CN O Br NH ј кон 2 HNNH, NH ex
plz help
Which aldehyde or ketone AND amine reactants are needed to complete the following reaction? CEO NaBH,CN Amine dil. H30+ N(CH3)3 NH(CH3 N(CH3)3 Predict the product(s) for the following reaction series: ОН -Br 1) NaH 2) ОН + -ONa A decapeptide that is part of an insulin-like peptide has the molecular formula: Asn, Arg(2), Ser(3), Phe, Cys, Leu, Thr. After partial hydrolysis, the fragments are: Cys-Ser-Phe-Ser- Arg-Asn-Ser-Cys Thr-Leu-Arg Ser-Thr What is the sequence? Ser-Phe-Ser-Thr-Leu-Arg-Arg-Asn-Ser-Cys Ser-Thr-Arg-Asn-Ser-Cys-Ser-Phe-Ser- Asn Arg-Asn-Ser-Cys-Ser-Phe-Ser-Thr-Leu-Arg Thr-Leu-Arg-Asn-Ser-Cys-Ser-Phe-Ser-Phe
pts) Give the missing reagents, reactants or products in the following reactions: (each box or blank iš U. 1. give name only give name only SOCI2 H2CRO4 1. ВНз H, heat (Fischer Esterification) 2. H202, HO Он propene + AICI3 (F.C. acyla give structure and IUPAC name: Br2/FeBr3
3. Provide a full arrow-pushing mechanism for each of the following reactions. Но, он НО Но он і - H- 0ң но он Насо, осна Нt H2O 4. A researcher wants to run the following sequence of reactions. However, they know starting Grignard reagent cannot exist due to the presence of its reactive carbonyl group. MgBr H.H cannot exist! An acetal group can be used to protect" a carbonyl from attack, allowing it to survive otherwise incompatible reaction conditions. Provide...
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