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Show Timer Question Completion Status: Name each of the reactions below by placing the number of...
1) Name each of the following organic compounds: (a-b-c-e-f-g-j-k-I-m-n) a) CH3CH2CH2CH3 j) CH3CHBOCHBrCH3 b) CH3CH2CH2C(CH3)3 c)...
1) Name each of the following organic compounds: (a-b-c-e-f-g-j-k-I-m-n) a) CH3CH2CH2CH3 j) CH3CHBOCHBrCH3 b) CH3CH2CH2C(CH3)3 c) CH2=CHCH2CH2CH3 d) CH3CHCICH(CH3)2 k) CH2BrCH(CH3)CHCICH2CH3 1) CH2CH(OH)CH(CH3)2 m) (CH3)2CHCHO n) CH3CH2CH2COCH3 e) (CH3)2C(OH)CH2CH3 f) CH3CHO o) (CH3)2CHCOOH p) CH3CH2CN g) CH3CH2COCH2CH3 h) CH3CH2COOH 9) CH3CHBCH(OH)CH3 i) CH3CH(OH)CH2CHO r) CH3COCH(CH3)CHBCH3
Section 4. Total points 26 1. Give one example of each of the following name reactions....
Section 4. Total points 26 1. Give one example of each of the following name reactions. For each reaction, you MUST INCLUDE: i) IUPAC Name of the reactant ii) IUPAC Name of the product iii) Reagents and reaction conditions (4points X 4 = 16 points) a. H.V.Z reaction b. Crossed aldol reaction between an aldehyde and a ketone 2-Propanone Benzaldehple c. Michael reaction between an a.ß unsaturated aldehyde and a B-diketone. d. Dieckman Condensation to have a cyclic product with...
Propose a synthesis of the compound below. Use one of the two starting materials and any...
Propose a synthesis of the compound below. Use one of the two starting materials and any of the reagents in the table. H2C=CHCH2CH2CCH3 Reagents available Starting materials CHCHBO n Br 유 1. CH3CCH2CO E 2 CHCOMEN)2 Br a. CH, Br b. CH3CH2Br Br Br Br | Br Br Br Br CH,Br 1. BrCH CH Br CH,Br 9. BI Br m r. HjO", heat 3. NaOCHy/C,H,OH h Br CHBO Br List the number of the starting material and then the letters...
Question 6 (1 point) Which of the following can be prepared by acetoacetic ester synthesis? CO,...
Question 6 (1 point) Which of the following can be prepared by acetoacetic ester synthesis? CO, 1 Question 7 (1 point) What is the order of acid strength from strongest to weakest acid? floath the oth OA) 2>1>4>3 OB) 1>2>3>4 C) 3>4>1>2 D) 2>4>1>3 O R H V B N Question 8 (1 point) What is the IUPAC name for this compound? COH CH,CH,CHCH,CH.CH O2-Ethyl-2-propyl-acetic acid 3-Hexylcarboxylic acid 2 Ethylpentanoic acid 2-Propylbutanoic acid Question 9 (1 point) 16 O 7...
RAH CC + (CH) Cả b. Be o RC + 2 CH3NH, CH.CH OH OCHO +...
RAH CC + (CH) Cả b. Be o RC + 2 CH3NH, CH.CH OH OCHO + CHCH,OH Habys o doronde TNHH R OH + CH3CHÚNH OH – Donc logo 1. CH3MgBr CH CH CH.CH2. Hy0 3-pentanone + (CH.CH) Culi- R acyl chloride h ITSE HCI R + R(H) CON excess 1. (CHCHCH2), AIH-78 °C 2. H20 CH,CH,CHOCH, 1. NaBHA RCEN 2. H2O NaBHA RC=CR Section 4. Total points 26 1. Give one example of each of the following name reactions....
Synthesis using Carbonyla-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry....
Synthesis using Carbonyla-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. My two target molecules are number 2 and number 12 in the last page. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the...
practice questions ③ show the product on products Expected for the reactions below a) + CH₃OH...
practice questions
③ show the product on products Expected for the reactions below a) + CH₃OH alcohol c-c-c aldehyde c-c-c acid C b) 014 + CH3 CH alcohol ÖH c) -10 kmnog LOH heat (Excess) cox - Bonus! 0: CEN: d) -10- H₂ Pd/c. (Excess H2) (Red) H -Bones! e) ÖH ć. + -10 alcohol он acid croch Grid x + CH₃ CH₂ 0 4 (drohol) -10 NH₂ 3 continued - show prodoct (s) رخ دن 2) 15 PH:10 NaOH...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
**(left structure)****(right structure)** The two structures for the assignment are above and the task is: 1....
**(left structure)****(right
structure)**
The two structures for the assignment are above and
the task is:
1. Perform a retrosynthetic analysis on the two target
molecules assigned to you. In each case the organic
starting material (what you have to work backwards toward) depends
upon the target. For the structure given above (structure on left),
the starting material is either malonic ester or acetoacetic ester
and any halide. For the structure given above (structure on right),
the starting material is any...
thats all the information that he gave us to solve the question. Thank you for trying...
thats all the information that he gave us to solve the question.
Thank you for trying anyways
X C E Question 23 1 pts The free-energy changes for the transfer of individual amino acid residues from a hydrophobic to an aqueous environment are given as follows: Amino acid AG of transfer (kJ/mol Proline -0.8 -12.6 Histidine 6.7 Alanine Methionine 14.3 Based on this information, which of these amino acid pairs is MOST likely to be represented in membrane-spanning alpha helices?...
1) Name each of the following organic compounds: (a-b-c-e-f-g-j-k-I-m-n) a) CH3CH2CH2CH3 j) CH3CHBOCHBrCH3 b) CH3CH2CH2C(CH3)3 c) CH2=CHCH2CH2CH3 d) CH3CHCICH(CH3)2 k) CH2BrCH(CH3)CHCICH2CH3 1) CH2CH(OH)CH(CH3)2 m) (CH3)2CHCHO n) CH3CH2CH2COCH3 e) (CH3)2C(OH)CH2CH3 f) CH3CHO o) (CH3)2CHCOOH p) CH3CH2CN g) CH3CH2COCH2CH3 h) CH3CH2COOH 9) CH3CHBCH(OH)CH3 i) CH3CH(OH)CH2CHO r) CH3COCH(CH3)CHBCH3
Section 4. Total points 26 1. Give one example of each of the following name reactions. For each reaction, you MUST INCLUDE: i) IUPAC Name of the reactant ii) IUPAC Name of the product iii) Reagents and reaction conditions (4points X 4 = 16 points) a. H.V.Z reaction b. Crossed aldol reaction between an aldehyde and a ketone 2-Propanone Benzaldehple c. Michael reaction between an a.ß unsaturated aldehyde and a B-diketone. d. Dieckman Condensation to have a cyclic product with...
Propose a synthesis of the compound below. Use one of the two starting materials and any of the reagents in the table. H2C=CHCH2CH2CCH3 Reagents available Starting materials CHCHBO n Br 유 1. CH3CCH2CO E 2 CHCOMEN)2 Br a. CH, Br b. CH3CH2Br Br Br Br | Br Br Br Br CH,Br 1. BrCH CH Br CH,Br 9. BI Br m r. HjO", heat 3. NaOCHy/C,H,OH h Br CHBO Br List the number of the starting material and then the letters...
Question 6 (1 point) Which of the following can be prepared by acetoacetic ester synthesis? CO, 1 Question 7 (1 point) What is the order of acid strength from strongest to weakest acid? floath the oth OA) 2>1>4>3 OB) 1>2>3>4 C) 3>4>1>2 D) 2>4>1>3 O R H V B N Question 8 (1 point) What is the IUPAC name for this compound? COH CH,CH,CHCH,CH.CH O2-Ethyl-2-propyl-acetic acid 3-Hexylcarboxylic acid 2 Ethylpentanoic acid 2-Propylbutanoic acid Question 9 (1 point) 16 O 7...
RAH CC + (CH) Cả b. Be o RC + 2 CH3NH, CH.CH OH OCHO + CHCH,OH Habys o doronde TNHH R OH + CH3CHÚNH OH – Donc logo 1. CH3MgBr CH CH CH.CH2. Hy0 3-pentanone + (CH.CH) Culi- R acyl chloride h ITSE HCI R + R(H) CON excess 1. (CHCHCH2), AIH-78 °C 2. H20 CH,CH,CHOCH, 1. NaBHA RCEN 2. H2O NaBHA RC=CR Section 4. Total points 26 1. Give one example of each of the following name reactions....
Synthesis using Carbonyla-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. My two target molecules are number 2 and number 12 in the last page. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the...
practice questions
③ show the product on products Expected for the reactions below a) + CH₃OH alcohol c-c-c aldehyde c-c-c acid C b) 014 + CH3 CH alcohol ÖH c) -10 kmnog LOH heat (Excess) cox - Bonus! 0: CEN: d) -10- H₂ Pd/c. (Excess H2) (Red) H -Bones! e) ÖH ć. + -10 alcohol он acid croch Grid x + CH₃ CH₂ 0 4 (drohol) -10 NH₂ 3 continued - show prodoct (s) رخ دن 2) 15 PH:10 NaOH...
Page 1 Synthesis using Carbonyl O-Substitution Chemistry Preamble This experiment involves the synthesis of target molecules using a-substitution chemistry. You are assigned two target molecules, one of which is best synthesized by an alkylation approach, while the other is best synthesized by an addition or condensation approach. You must do the following: 1. Perform a retrosynthetic analysis on the two target molecules assigned to you. In each case the organic starting material (what you have to work backwards toward) depends...
**(left structure)****(right
structure)**
The two structures for the assignment are above and
the task is:
1. Perform a retrosynthetic analysis on the two target
molecules assigned to you. In each case the organic
starting material (what you have to work backwards toward) depends
upon the target. For the structure given above (structure on left),
the starting material is either malonic ester or acetoacetic ester
and any halide. For the structure given above (structure on right),
the starting material is any...
thats all the information that he gave us to solve the question.
Thank you for trying anyways
X C E Question 23 1 pts The free-energy changes for the transfer of individual amino acid residues from a hydrophobic to an aqueous environment are given as follows: Amino acid AG of transfer (kJ/mol Proline -0.8 -12.6 Histidine 6.7 Alanine Methionine 14.3 Based on this information, which of these amino acid pairs is MOST likely to be represented in membrane-spanning alpha helices?...
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