Homework Answers
Both reactions are Nucleophilic addition elimination reaction of C= O group.
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8 Predict the major product(s) formed when hexanoyl chloride is treated with each of...
1. Predict the major product(s) formed when hexanoyl chloride is treated with excess EtMgBr, followed by...
1. Predict the major product(s) formed when hexanoyl chloride is
treated with excess EtMgBr, followed by H2O.
2. Predict the major product(s) formed when hexanoyl chloride is
treated with Et2CuLi.
3. Predict the major product(s) formed when hexanoyl chloride is
treated with C6H5CO2Na.
4. Predict the major product(s)
formed when hexanoyl chloride is treated with excess
NH3.
5.
19.54 predict the major product(s) from the treatment of acetone with the following: 19.54 Predict the...
19.54 predict the major product(s) from the treatment
of acetone with the following:
19.54 Predict the major product(s) from the treatment of acetone with the following: (a) [H*1, NH3, (-H2O) (b) [H*], CH3NH2, (-H2O) (d) [H*], (CH3)2NH, (-H2O) (c) [H*], excess ETOH, (-H2O) (e) [H*], NH2NH2, (-H2O) (f) [H*1, NH2OH, (-H2O) (g) NaBH4, MeOH (h) RCO3H (i) HCN, KCN () EtMgBr followed by H2O (k) (C&Hs)3P=CHCH2CH3 (I) LIAIH4 followed by H2O
2. Predict the product. CH,CHINH Or . 1. excess CH 1 2. Ag,0,H,O heat 5. Match...
2. Predict the product. CH,CHINH Or . 1. excess CH 1 2. Ag,0,H,O heat 5. Match the reagents to the corresponding reaction. G. H20 H. xs CH3CH2NH2 A. SOCI2, pyridine B. Ethanol, pyridine C. 1) xs LAH 2) H20 D. 1) xs CH,CHMgBr 2) H30 E. 1) NaOH 2) H30* F. 1) DIBAH 2) H20 1. 1) LiAl(OR)2) H20 J. (CH2CH2) Culi K. xs NH3 L. 1) NaOH 2) CHÚCHỊCHÚCOCI M. Butanol, H
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...
E to H please I. Predict the major organic product formed in the following reactions a)...
E to H please
I. Predict the major organic product formed in the following reactions a) o KOBut HOBut b) KOBut HOBut öt CH CH; CH_CH CH KCN Acetone н d) solvent alkyl halide nucleophile CH e) H -Br KOBut HOBu' Br- -H CH f) Br CH,CH OH two products formed ♡ + CHI h) Br NaOCH3
TsCl, pyridine 1TSCI, pyridine, 2) LiAlH Draw the major product formed when 2-pentanol is treated with...
TsCl, pyridine 1TSCI, pyridine, 2) LiAlH Draw the major product formed when 2-pentanol is treated with each reagent(s) 1) H2SO4, A 2) O, 3) Zn, H2O 4. PCC a е b Jones Reagent (Chromic acid + acetone) НСІ 1) H.SO4, A Devise a synthesis of each compound from acetylene (HC= CH) and organic compounds containing two carbons or less. You may use any other required reagents CH, CHCH&CH 5. a CH CHCH-CH,ОН b CH CHCH,CHО cis CH CH2CH-CHCH CO>H d...
Predict the products formed in the following reactions. Predict the product(s) formed in the following reactions....
Predict the products formed in the following reactions.
Predict the product(s) formed in the following reactions. If there is no reaction, write “No Rxn" as the answer for the major product and leave the minor product box blank. If there is no minor product in the reaction, then leave the minor product box blank. If there are multiple products, make sure the products are in the appropriate box. (24 points, 4 points each) Note: Do not over complicate some questions...
Predict the major product formed when the compounds shown below react with each other in the...
Predict the major product formed when the compounds shown below
react with each other in the presence of AlCl3 and then
H2O.
2. Draw the major product(s) formed when the optically active compound shown below is treated with...
2. Draw the major product(s) formed when the optically active compound shown below is treated with H2O/H2SO4. Is the product optically active? Why or why not? (4 pts) optically active
1. 2. Predict the major organic product formed when the compounds shown below undergo a reaction...
1.
2.
Predict the major organic product formed when the compounds shown below undergo a reaction in the presence of AICI3 Interactive 3D display mode OiPr Cl Нас CH3 СНз 3 Choose the right reagent or series of reagents from the ones listed to carry out the following synthesis (see picture). CH он CN followed by HCl, H2O, A, then NBS, A, peroxide NBS, A, peroxide, followed by HCOOH, NBS, A, peroxide, followed by HCl, H2O, A, then CN o...
1. Predict the major product(s) formed when hexanoyl chloride is
treated with excess EtMgBr, followed by H2O.
2. Predict the major product(s) formed when hexanoyl chloride is
treated with Et2CuLi.
3. Predict the major product(s) formed when hexanoyl chloride is
treated with C6H5CO2Na.
4. Predict the major product(s)
formed when hexanoyl chloride is treated with excess
NH3.
5.
19.54 predict the major product(s) from the treatment
of acetone with the following:
19.54 Predict the major product(s) from the treatment of acetone with the following: (a) [H*1, NH3, (-H2O) (b) [H*], CH3NH2, (-H2O) (d) [H*], (CH3)2NH, (-H2O) (c) [H*], excess ETOH, (-H2O) (e) [H*], NH2NH2, (-H2O) (f) [H*1, NH2OH, (-H2O) (g) NaBH4, MeOH (h) RCO3H (i) HCN, KCN () EtMgBr followed by H2O (k) (C&Hs)3P=CHCH2CH3 (I) LIAIH4 followed by H2O
2. Predict the product. CH,CHINH Or . 1. excess CH 1 2. Ag,0,H,O heat 5. Match the reagents to the corresponding reaction. G. H20 H. xs CH3CH2NH2 A. SOCI2, pyridine B. Ethanol, pyridine C. 1) xs LAH 2) H20 D. 1) xs CH,CHMgBr 2) H30 E. 1) NaOH 2) H30* F. 1) DIBAH 2) H20 1. 1) LiAl(OR)2) H20 J. (CH2CH2) Culi K. xs NH3 L. 1) NaOH 2) CHÚCHỊCHÚCOCI M. Butanol, H
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...
E to H please
I. Predict the major organic product formed in the following reactions a) o KOBut HOBut b) KOBut HOBut öt CH CH; CH_CH CH KCN Acetone н d) solvent alkyl halide nucleophile CH e) H -Br KOBut HOBu' Br- -H CH f) Br CH,CH OH two products formed ♡ + CHI h) Br NaOCH3
TsCl, pyridine 1TSCI, pyridine, 2) LiAlH Draw the major product formed when 2-pentanol is treated with each reagent(s) 1) H2SO4, A 2) O, 3) Zn, H2O 4. PCC a е b Jones Reagent (Chromic acid + acetone) НСІ 1) H.SO4, A Devise a synthesis of each compound from acetylene (HC= CH) and organic compounds containing two carbons or less. You may use any other required reagents CH, CHCH&CH 5. a CH CHCH-CH,ОН b CH CHCH,CHО cis CH CH2CH-CHCH CO>H d...
Predict the products formed in the following reactions.
Predict the product(s) formed in the following reactions. If there is no reaction, write “No Rxn" as the answer for the major product and leave the minor product box blank. If there is no minor product in the reaction, then leave the minor product box blank. If there are multiple products, make sure the products are in the appropriate box. (24 points, 4 points each) Note: Do not over complicate some questions...
Predict the major product formed when the compounds shown below
react with each other in the presence of AlCl3 and then
H2O.
2. Draw the major product(s) formed when the optically active compound shown below is treated with H2O/H2SO4. Is the product optically active? Why or why not? (4 pts) optically active
1.
2.
Predict the major organic product formed when the compounds shown below undergo a reaction in the presence of AICI3 Interactive 3D display mode OiPr Cl Нас CH3 СНз 3 Choose the right reagent or series of reagents from the ones listed to carry out the following synthesis (see picture). CH он CN followed by HCl, H2O, A, then NBS, A, peroxide NBS, A, peroxide, followed by HCOOH, NBS, A, peroxide, followed by HCl, H2O, A, then CN o...
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