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Homework Answers
All other reagents can not be used to produce an alcohol or have other reasons, so that it cannot be used here. For example:
Reagent A : Oxidizing reagent; used to convert alcohol into ketone or carboxylic acid.
Reagent B : Can be used to produce an alcohol, but the phenyl group (-C6H5) will attach in the product molecule.
Reagent C : Used in esterification reaction (carboxylic acid to carboxylic ester).
Reagent D : Reduces carbonyl compounds (aldehydes and ketones) to produce alcohols.
Reagent E : Used as a base in elimination reaction.
Reagent F : Called Wolff-Kishner
reagent. Used in the following conversion reaction -- 
.
Therefore the answer should be :
When 3-methyl-2-butanone is treated with reagent D, it will produce 3-methyl-2-butanol.
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Choose a starting material and a reagent (A-F) to synthesize the given product. When [Select] is...
Choose a starting material and a reagent (A-F) to synthesize the given product Choose a starting...
Choose a starting material and a reagent (A-F) to synthesize the
given product
Choose a starting material and a reagent (A-F) to synthesize the given product When [Select] is treated with [ Select] - it will produce 2,3-dimethyl-3-pentanol. REAGENTS Jones' reagent, CrO3 in H30(+) CH3MgBr (in ether) followed by H30(+) workup CH3OH (excess) acid-catalyst, heat (- H20) NaBH4 in CH3OH (CH2)5NH (piperidine) N2H4 KOH & strong acid-catalyst, heat (- heat H20)
choose a starting material (4-methyl-2-pentanone, 2-methyl-3-pentanone, 2,3-dimethylbutanal) and a reagent from A-F to synthesize 2,2-dimethoxy-4-methylpentane. Choose...
choose a starting material (4-methyl-2-pentanone,
2-methyl-3-pentanone, 2,3-dimethylbutanal) and a reagent from A-F
to synthesize 2,2-dimethoxy-4-methylpentane.
Choose a starting material and a reagent (A-F) to synthesize the given product. When [Select ] is treated with (Select ] it will produce 2,2-dimethoxy-4- methylpentane. REAGENTS C. A. Jones' reagent, Croz in CH3MgBr (in CH3OH ether) (excess) followed by acid-catalyst, H30(+) workup heat (-H20) H₂O(+) NaBH4 in CH3OH (CH2)5NH (piperidine) N2H4 KOH & acid-catalyst, strong heat heat (-H20)
Question 9.27, 9.30 Choose one reagent from the Table to carry out the following conversions. Use...
Question 9.27, 9.30 Choose one reagent from the Table to carry out the following conversions. Use letters from the table to specify reagents. Reagents КMnO,/ Н,о* O3 d 1. Br2 g a 2. KOH in ethanol H2/ Lindlar catalyst hr H20/ H2SO4/ HgSO4 е 1. NaNH2 in NH3 2. CH3Br Li in NH3 1 equiv Br2 f 1. BH3 in THF C 2. H202 in NaOH a) CHACH,сH,сH,CECH CHн-CH-CH-CH2CH-CH CHз b) сHa-CHa-CEс-сн, CH3CH2 The following synthesis requires more than one...
1. Which Wittig reagent would be used to synthesize 2 CH-CH=P(CAH) CH=P(CHẠh. P(CH3)3 CH,CH,CH-P(CH3)3 IV 2....
1. Which Wittig reagent would be used to synthesize 2 CH-CH=P(CAH) CH=P(CHẠh. P(CH3)3 CH,CH,CH-P(CH3)3 IV 2. What is the correct IUPAC name for the following compound? 6 eye 3. What is the correct structure for 7-methyl-4-octanone? 3 4. The products, D and E, of the following reaction sequence, S "CN HCI HCN CH.NO H20 heat would be: CH2CH2CN CH,CH,MgBe HO E ? ether Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents....
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List...
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List of Reagents -N:C:N- KMnO4, H2SO4 8 00 (CH3),COCOCOC(CH3)3 Ag(NH3)2+, 120 Fe, HCI KMnO4, NaOH, H2O, cold AlCl3 Bra (excess), NaOH (excess), H20 Brz, Fe Br2, H20 Br2, H2O, H3O+ Br2, hy Br2, NaOH (excess), H2O Br2, P Buli CF3CO,H CH;=0 Formaldehyde оо CH3COCCH o CH_CC1, pyridine H2, Lindlar's catalyst H2.Pd/C H2, Pa/C, high pressure H, Raney-Ni HANNH HENNH, KOH, (HOCH2CH2)20, heat H2O H20, H2SO4,...
please help in all sections asap!!!! Which of the following reagent(s) could not be used to...
please help in all sections asap!!!!
Which of the following reagent(s) could not be used to carry out the following transformation? HSCH2CH2SH, BFy; then Raney NI (H) 1. NH NH/H"; 2. KOH/H20/heat LAH, ether Zn(Hg), HCI Predict the product for the following reaction. О, Н excess 1. NH2NH2/H 2. KOH/ H2O/A NNH2 HO. Η ΝΗΝΗΣ NH2 CH OH CH CH HOCHNHNH OH NH2 NNH2 IN V We were unable to transcribe this imagePredict the product(s) for the following reaction. NaOH...
please help in all sections asap!! Predict the product for the following reaction sequence: MgBr PCO...
please help in all sections asap!!
Predict the product for the following reaction sequence: MgBr PCO CHCE etler Predict the product for the following reaction, Predict the product for the following reaction. excess CH3OH H2SO4 H3CO OCHз Но осна ОСН3 Which one of the following compounds will yield 1-hexanol when treated with butylmagnesium bromide followed by acid workup? 1-hexanol formaldehyde acetaldehyde odrane hexanal Provide the reagents necessary to carry out the following conversion. 1. H20/ H2SO4 2. PCC/CH2Cl2 PCC/ CH2Cl2...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyri...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepa...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
Can you help me identify reagent (i), Compound 8 and Compound 12 in the reaction scheme?...
Can you help me identify reagent (i), Compound 8 and
Compound 12 in the reaction scheme?
You have laboratory data on all the compounds in the
synthesis, however the amount of data available to you varies. Some
have the entirety of the spectral data, others have as little as
the elemental analysis. Use the laboratory data to help you
discover which reaction has been performed.
The lab data for Compound 8 and 12 is as
follows:
You can use any...
Choose a starting material and a reagent (A-F) to synthesize the
given product
Choose a starting material and a reagent (A-F) to synthesize the given product When [Select] is treated with [ Select] - it will produce 2,3-dimethyl-3-pentanol. REAGENTS Jones' reagent, CrO3 in H30(+) CH3MgBr (in ether) followed by H30(+) workup CH3OH (excess) acid-catalyst, heat (- H20) NaBH4 in CH3OH (CH2)5NH (piperidine) N2H4 KOH & strong acid-catalyst, heat (- heat H20)
choose a starting material (4-methyl-2-pentanone,
2-methyl-3-pentanone, 2,3-dimethylbutanal) and a reagent from A-F
to synthesize 2,2-dimethoxy-4-methylpentane.
Choose a starting material and a reagent (A-F) to synthesize the given product. When [Select ] is treated with (Select ] it will produce 2,2-dimethoxy-4- methylpentane. REAGENTS C. A. Jones' reagent, Croz in CH3MgBr (in CH3OH ether) (excess) followed by acid-catalyst, H30(+) workup heat (-H20) H₂O(+) NaBH4 in CH3OH (CH2)5NH (piperidine) N2H4 KOH & acid-catalyst, strong heat heat (-H20)
Question 9.27, 9.30 Choose one reagent from the Table to carry out the following conversions. Use letters from the table to specify reagents. Reagents КMnO,/ Н,о* O3 d 1. Br2 g a 2. KOH in ethanol H2/ Lindlar catalyst hr H20/ H2SO4/ HgSO4 е 1. NaNH2 in NH3 2. CH3Br Li in NH3 1 equiv Br2 f 1. BH3 in THF C 2. H202 in NaOH a) CHACH,сH,сH,CECH CHн-CH-CH-CH2CH-CH CHз b) сHa-CHa-CEс-сн, CH3CH2 The following synthesis requires more than one...
1. Which Wittig reagent would be used to synthesize 2 CH-CH=P(CAH) CH=P(CHẠh. P(CH3)3 CH,CH,CH-P(CH3)3 IV 2. What is the correct IUPAC name for the following compound? 6 eye 3. What is the correct structure for 7-methyl-4-octanone? 3 4. The products, D and E, of the following reaction sequence, S "CN HCI HCN CH.NO H20 heat would be: CH2CH2CN CH,CH,MgBe HO E ? ether Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents....
17. Use ANY needed reagents to effect the following transformation. (30 points) starting material product List of Reagents -N:C:N- KMnO4, H2SO4 8 00 (CH3),COCOCOC(CH3)3 Ag(NH3)2+, 120 Fe, HCI KMnO4, NaOH, H2O, cold AlCl3 Bra (excess), NaOH (excess), H20 Brz, Fe Br2, H20 Br2, H2O, H3O+ Br2, hy Br2, NaOH (excess), H2O Br2, P Buli CF3CO,H CH;=0 Formaldehyde оо CH3COCCH o CH_CC1, pyridine H2, Lindlar's catalyst H2.Pd/C H2, Pa/C, high pressure H, Raney-Ni HANNH HENNH, KOH, (HOCH2CH2)20, heat H2O H20, H2SO4,...
please help in all sections asap!!!!
Which of the following reagent(s) could not be used to carry out the following transformation? HSCH2CH2SH, BFy; then Raney NI (H) 1. NH NH/H"; 2. KOH/H20/heat LAH, ether Zn(Hg), HCI Predict the product for the following reaction. О, Н excess 1. NH2NH2/H 2. KOH/ H2O/A NNH2 HO. Η ΝΗΝΗΣ NH2 CH OH CH CH HOCHNHNH OH NH2 NNH2 IN V We were unable to transcribe this imagePredict the product(s) for the following reaction. NaOH...
please help in all sections asap!!
Predict the product for the following reaction sequence: MgBr PCO CHCE etler Predict the product for the following reaction, Predict the product for the following reaction. excess CH3OH H2SO4 H3CO OCHз Но осна ОСН3 Which one of the following compounds will yield 1-hexanol when treated with butylmagnesium bromide followed by acid workup? 1-hexanol formaldehyde acetaldehyde odrane hexanal Provide the reagents necessary to carry out the following conversion. 1. H20/ H2SO4 2. PCC/CH2Cl2 PCC/ CH2Cl2...
Hc VCH Draw the organic product formed when CH3CH2CH2OH is treated with each reagent. a H2S04 (180°C) d SOC12, pyridine Ig 1) NaH; 2) CH3CH2Br b NaH e PBr3 h 1) TSCI, pyridine; 2) NaSH c HBr f TsCl, pyridine 3. Draw the organic product formed when l-methylcyclohexanol is treaded with each reagent. In some cases, no reaction occurs. a KH c HBr Te NaHCO3 b Nacid HCI f 1) KH; 2) CH3CH2Br Draw two different routes to each of...
i need help with the postlab questions please
Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....
Can you help me identify reagent (i), Compound 8 and
Compound 12 in the reaction scheme?
You have laboratory data on all the compounds in the
synthesis, however the amount of data available to you varies. Some
have the entirety of the spectral data, others have as little as
the elemental analysis. Use the laboratory data to help you
discover which reaction has been performed.
The lab data for Compound 8 and 12 is as
follows:
You can use any...
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