Homework Answers
Add Answer to:
2. Show the step(s) necessary to transform the compound on the left into the acid on...
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 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: 9 сн,сессн,дося, CH3C=CCH2COH b) CHÚC-CCH,lona* CH?C=CCHąČN(CH2CH_CH3)2 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. CH,C=COH CH3C=CCH2OH 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOC12. a) CH;C=CCH,COH - снсесснRocнск b) CH3C=CCH_COH » CHỤC=CCHCNCH) ber these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. O...
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...
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. Show how to transform the compound on the left into the compound on the right.
1. Show how to transform the compound on the left into the compound on the right. Several steps will be involved. You may use any additional organic or inorganic compounds you wish.2. Draw all resonance contributors to this radical. If there are no others, write 'None". 3. Write in all the products of this reaction: 4. Label all carbons in this molecule as to whether they are 1°, 2° or 3° 5. Draw in all vinyl H's (if any) with the subscript 'v" this way: HyDraw...
Provide the major product(s) for the following reactions: Show Stereochemistry when necessary (9 points total) HBr...
Provide the major product(s) for the following reactions: Show Stereochemistry when necessary (9 points total) HBr (1 equivalent) HBr (2 equivalents) Br2 Brz (1 equivalent) CH,CI, (2 equivalents) CH,CI, HO 1) disyamylborane HgSo., H2SO4 2) H0, NaOH, H2O Bonus: Provide the major product(s) for the following reactions: Show Stereochemistry when necessary (4 points total) 1) NaNH, (1) NaNH, 2) (CH),CHCH,Br 2) (CH),CHCH,Br 3) H, 3) L, NH, Lindlar's catalyst 1) NaNH, 2) EtBr 3) Hz, Pd/C 1) NaNH, 2) EtBr...
#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?...
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 these compounds: 9 сн,сессн,дося, CH3C=CCH2COH b) CHÚC-CCH,lona* CH?C=CCHąČN(CH2CH_CH3)2 2. Show the step(s) necessary to transform the compound on the left into the acid on the right. CH,C=COH CH3C=CCH2OH 3. Show the steps necessary to transform the acid on the left into the compound on the right. Be sure to use SOC12. a) CH;C=CCH,COH - снсесснRocнск b) CH3C=CCH_COH » CHỤC=CCHCNCH) ber these in order of ease of hydrolysis. 1 = easiest to hydrolyze, 4 = hardest to hydrolyze. O...
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...
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
Provide the major product(s) for the following reactions: Show Stereochemistry when necessary (9 points total) HBr (1 equivalent) HBr (2 equivalents) Br2 Brz (1 equivalent) CH,CI, (2 equivalents) CH,CI, HO 1) disyamylborane HgSo., H2SO4 2) H0, NaOH, H2O Bonus: Provide the major product(s) for the following reactions: Show Stereochemistry when necessary (4 points total) 1) NaNH, (1) NaNH, 2) (CH),CHCH,Br 2) (CH),CHCH,Br 3) H, 3) L, NH, Lindlar's catalyst 1) NaNH, 2) EtBr 3) Hz, Pd/C 1) NaNH, 2) EtBr...
#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?...
Most questions answered within 3 hours.
-
1a) According to the ideal gas law, _______________.
a. a gas has infinite volume at absolute...
asked 9 minutes ago -
Oakdale Fashions, Inc. had $245,000 in 2018 taxable income.
Using the tax schedule in Table 2.3...
asked 32 minutes ago -
The marketing class at CSUS had an average score of 150. An
educational analyst determined that...
asked 1 hour ago -
Justin Case has purchased a $250 000 home by putting 20 % down
and taking out...
asked 2 hours ago -
1. In a labor market, marginal cost for a firm is
____________.
a. recruiting cost
b....
asked 2 hours ago -
On January 1, 2019, ABC Company issued $60,000,000 of 20-year,
10.5% bonds when the market rate...
asked 2 hours ago -
39.4% of US homes continue to use a landline in addition to cell
phone service. 3...
asked 3 hours ago -
Starting with benzene, synthesize 1-phenyl-1-butyne.
Show intermediates and reagents.
asked 4 hours ago -
Create a 32-run crossed array design with six control factors
and two noise factors such that...
asked 5 hours ago -
A 500g sample of sand from source A has the following amounts
retained on each sieve....
asked 5 hours ago -
In
your own words, please explain the essay by John Keynes wrote "The
End of Laissez...
asked 5 hours ago -
How are the matrix and pixels related? Why are smaller
pixels better for diagnostic quality?
asked 5 hours ago