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1. Name these compounds: 9 сн,сессн,дося, CH3C=CCH2COH b) CHÚC-CCH,lona* CH?C=CCHąČN(CH2CH_CH3)2 2. Show the step(s) ne...
1. Name these compounds: *) HOSCH.HCH o cuddChuquichs b) Na - PCHCHICH " CH CH.CH)ÇUCH сн;...
1. Name these compounds: *) HOSCH.HCH o cuddChuquichs b) Na - PCHCHICH " CH CH.CH)ÇUCH сн; 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. 1-pentanol → pentanoic acid 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. pentanoic acid isopropyl pentanoate pentanoic acid N-phenylpentanamide 4. Number these in order of ease of hydrolysis. 1 - easiest...
2. Show the step(s) necessary to transform the compound on the left into the acid on...
2. Show the step(s) necessary to transform the compound on the left into the acid on the right. HOCH CH CH Br + HOCH2CH2CH,COH 19 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) H2C=CHCH_COH – H.C-chch_Coch; H2C=CHCH COH H2C=CHCHÖNCHS CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. CH;CH&CI CH,CHUCNHC,H, NCCH, CHOCCH,
3. Show the steps necessary to transform the acid on the left into the compound on...
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) CH2COH Cl b) Cl 4. Number these in order of ease of hydrolysis. 1 -easiest to hydrolyze, 4- hardest to hydrolyze. EN Cl
3. Show the steps necessary to transform the acid on the left into the compound on...
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCI2 a) -CHCHOCH Р-снсн. Сон Н.С-СНСH,CoСНB Н-С-СНCH,COН несиси вусая, b) Н.С-СНСH,CоН нсснсн 2он Н,С-СНСH,CNСАНЯ CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 =easiest to hydrolyze, 4 hardest to hydrolyze. сHсн2нся. сновсм, CH2CH2CNHC&Hs CHоёсн, CH3CH2CCI N=CCH3
1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound...
1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound on the left into the acid on the right. chlorobenzene benzoic acid 3. What are the products of the following reaction? H:0* 4. Write in the product of this reaction: H2O C6H5CH2C=N ------ H. heat 5. Which type of spectroscopy (IR, 'H NMR, and/or SC NMR) would be good to distinguish between acetonitrile and acetic acid? State what you would observe for each compound in...
1. Name this compound, including stereochemistry: НО CHCHCH,ОН 2. Show the step(s) necessary to transform the...
1. Name this compound, including stereochemistry: НО CHCHCH,ОН 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. Benzyl alcohol benzoic acid 3. What are the products of the following reaction? H30 CHO OCH3 -
1. Name this compound, including stereochemistry: НОС CoHs HOC 2. Show the step(s) necessary to transform...
1. Name this compound, including stereochemistry: НОС CoHs HOC 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. Methoxybenzene p-methoxybenzoic acid 3. What are the products of the following reaction? OCH3 Н,о* OCH3
1. Draw structures for the following compounds: a) l-ethyl-2-methylcyclohexane b) 4-methyl hexanal c) N-N-dimethylpentanamide 2. What...
1. Draw structures for the following compounds: a) l-ethyl-2-methylcyclohexane b) 4-methyl hexanal c) N-N-dimethylpentanamide 2. What is the product of this bromination reaction? H2C-CH=CH-CH2-CH2-CH3 + Br2 3. What is the product of this oxidation reaction? OH H3C-CH-CH-CHg 10 Сн, 4. Consider the esterification reaction reaction below: H, SO H3C-CH2-CH2-CH2-C-OH + H2C-CH2-OH What organic compound is the reactant on the left? What organic compound is the reactant on the right? Draw the product of the reaction. What type of organic compound...
#1-5. Dr. Hellwig OMEWORK 5 Chem 204 Name this compound, including stereochemistry: 1. cCoCt носс-сСH,ОСHS 2....
#1-5.
Dr. Hellwig OMEWORK 5 Chem 204 Name this compound, including stereochemistry: 1. cCoCt носс-сСH,ОСHS 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. m-methoxytoluene m-methoxybenzoic acid 3. What are the products of the following reaction? Но" Write in the product of this reaction: 4 Н.о H2C=CHCH2C N H', heat 5. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between acetonitrile and benzoic acid?...
1. Name these compounds: *) HOSCH.HCH o cuddChuquichs b) Na - PCHCHICH " CH CH.CH)ÇUCH сн; 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. 1-pentanol → pentanoic acid 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. pentanoic acid isopropyl pentanoate pentanoic acid N-phenylpentanamide 4. Number these in order of ease of hydrolysis. 1 - easiest...
2. Show the step(s) necessary to transform the compound on the left into the acid on the right. HOCH CH CH Br + HOCH2CH2CH,COH 19 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) H2C=CHCH_COH – H.C-chch_Coch; H2C=CHCH COH H2C=CHCHÖNCHS CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. CH;CH&CI CH,CHUCNHC,H, NCCH, CHOCCH,
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCl2. a) CH2COH Cl b) Cl 4. Number these in order of ease of hydrolysis. 1 -easiest to hydrolyze, 4- hardest to hydrolyze. EN Cl
3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOCI2 a) -CHCHOCH Р-снсн. Сон Н.С-СНСH,CoСНB Н-С-СНCH,COН несиси вусая, b) Н.С-СНСH,CоН нсснсн 2он Н,С-СНСH,CNСАНЯ CH2CH2CH3 4. Number these in order of ease of hydrolysis. 1 =easiest to hydrolyze, 4 hardest to hydrolyze. сHсн2нся. сновсм, CH2CH2CNHC&Hs CHоёсн, CH3CH2CCI N=CCH3
1. Name this compound, including stereochemistry: HOCCECCH,CH Show the step(s) necessary to transform the compound on the left into the acid on the right. chlorobenzene benzoic acid 3. What are the products of the following reaction? H:0* 4. Write in the product of this reaction: H2O C6H5CH2C=N ------ H. heat 5. Which type of spectroscopy (IR, 'H NMR, and/or SC NMR) would be good to distinguish between acetonitrile and acetic acid? State what you would observe for each compound in...
1. Name this compound, including stereochemistry: НО CHCHCH,ОН 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. Benzyl alcohol benzoic acid 3. What are the products of the following reaction? H30 CHO OCH3 -
1. Name this compound, including stereochemistry: НОС CoHs HOC 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. Methoxybenzene p-methoxybenzoic acid 3. What are the products of the following reaction? OCH3 Н,о* OCH3
1. Draw structures for the following compounds: a) l-ethyl-2-methylcyclohexane b) 4-methyl hexanal c) N-N-dimethylpentanamide 2. What is the product of this bromination reaction? H2C-CH=CH-CH2-CH2-CH3 + Br2 3. What is the product of this oxidation reaction? OH H3C-CH-CH-CHg 10 Сн, 4. Consider the esterification reaction reaction below: H, SO H3C-CH2-CH2-CH2-C-OH + H2C-CH2-OH What organic compound is the reactant on the left? What organic compound is the reactant on the right? Draw the product of the reaction. What type of organic compound...
#1-5.
Dr. Hellwig OMEWORK 5 Chem 204 Name this compound, including stereochemistry: 1. cCoCt носс-сСH,ОСHS 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. m-methoxytoluene m-methoxybenzoic acid 3. What are the products of the following reaction? Но" Write in the product of this reaction: 4 Н.о H2C=CHCH2C N H', heat 5. Which type of spectroscopy (IR, 'H NMR, and/or C NMR) would be good to distinguish between acetonitrile and benzoic acid?...
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