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Give the structures of E to H showing the position of the labelled carbon [*] in...
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne ...
Draw structures corresponding to the following names:
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
4. Draw structures corresponding to the following systematic names; a) 1-isopropyl-4-methylcyclohexene b) 3-butyl-2-heptene c) 4-methyl-1,2- hexadiene...
4. Draw structures corresponding to the following systematic names; a) 1-isopropyl-4-methylcyclohexene b) 3-butyl-2-heptene c) 4-methyl-1,2- hexadiene d) trans-3,3-dimethyl-4-propyl-1,5-octadiene e) (42)-2,4-diethyl-1,4-hexadiene f) 1.2-propadiene g) (32,5E) -2,6-dimethyl-1,3,5,7-octatetraene h) cis-2,2,5,5-tetramethyl-3-hexene i) Methylenecyclohexane, j) trans- 1,2 divinylcyclohexane
please answer d e f g For each of the following structures: (a) Give the IUPAC...
please answer d e f g
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3- (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose...
PLEASE HELP WITH ALL QUESTIONS QUESTION 1 1.1 Draw a fully-labelled diagram showing the process of...
PLEASE HELP WITH ALL QUESTIONS
QUESTION 1 1.1 Draw a fully-labelled diagram showing the process of conjugation in Spirogyra. (10) 1.2 List FOUR advantages and FOUR disadvantages of algae. (8) 1.3 Name the different terrestrial biomes of the world and give one diagnostic characteristic of each biome. (12) [30] QUESTION 2 2.1 By means of a labelled diagram, describe the life cycle of an angiosperm. Use blocks of information to explain each stage. (15) 2.2 What are the advantages and...
1Ozonolysis of alkenes yields Alcohol carboxylic acid b-ketones if one of the unsaturated carbon atoms is...
1Ozonolysis of alkenes yields Alcohol carboxylic acid b-ketones if one of the unsaturated carbon atoms is disubstituted d- alkane 23-Aldehyde C-0 is more polarized than ketone C-O because a-As in carbocations, more alkyl groups stabilize + character b-Ketone has more alkyl groups, stabilizing the C-O carbon inductively c- due to a andb d- none of the above 24-Aldehydes and unhindered ketones react with HCN to form a-Cyanohydrine b-alcohol c- alkyne d- alkene 25-addition of a Grignard reagent to formaldehyde followed...
Examine structures E through H below to answer questions three and four. Onlar onlarowa 3) All four of the struct...
Examine structures E through H below to answer questions three and four. Onlar onlarowa 3) All four of the structures (E through H) above are insoluble in water. Which of the structures would you expect to become more soluble in water when combined with HCl(aq), and WHY? 4) Which of the structures (E through H) above would you expect to form a salt when mixed with - aqueous sodium hydroxide, and WHY?
as A Questions 1-4 refers to the five titration curves (labelled mL of titrant mL of...
as A Questions 1-4 refers to the five titration curves (labelled mL of titrant mL of titrant ml of titrant mL of titrant mL of titrant 1 Which curve shows the titration of a strong acid with a strong base? AA BB CC DD EE Fnone of the above 2 Which curve shows the titration of a weak acid with a strong base? A A BB CC DD EE Fnone of the above 3 Which curve shows the titration of...
write condensed structures fore each of the following compounds Homework Problems 7.1 Write condensed structures for...
write condensed structures fore each of the following
compounds
Homework Problems 7.1 Write condensed structures for each of the following compounds: a. 2,2,4-trimethylpentane b. 5-isopropyl-2-methyloctane c. 1,1,3,3-tetrabromopropane d. 1,1-dichlorocyclopentane e. 1,4-diethylcyclohexane f. 1-bromo-2-methylcyclobutane What are the IUPAC names of the following compounds? 7.2 CH2CH, CH3 a) CH, C CH, CH, CH СH,CH, сн, CH2CH, b) CH2CH d) (CH),CCH2CH e) F Br Br Write the structural formulas and names for FOUR isomers of cycloalkane, CSH10. 7.3 7.4 Propose structures for molecules...
identify which compound is more acidic and explain your choice. or each of the following compounds,...
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
Draw correct. condens Cyclic portions of structures condensed structures for the following compounds according to IUPAC...
Draw correct. condens Cyclic portions of structures condensed structures for the following compounds according to IUPAC rules portions of structures can be done as line-angle drawings (20 pts.) b) |-ethyl-2-methylcyclohexane a) 1.1.2-trichloro-2-fluoropropane d) cis-4,4,5,5-tetramethyl-2-hexene 3-ethyl-2,2,3-trimethyloctane 3,3-dimethyl-1-octyne 4-ethyl-2-heptene 8) 1-chloro-2-propyleyelopropane h) 1,2,4-tribromo-3-chlorocyclohexane i) trans-4-ethyl-2-octene i) 1-bromo-1-chlorocycloheptane 3) hake 1-bromopentane as the only product from the reaction of 1-pentene with Can you easily make 1-bromopentane as the HBr and why? (Explain!) (10 pts.) (HINT: You may want to draw out a chemical...
Draw structures corresponding to the following names:
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
4. Draw structures corresponding to the following systematic names; a) 1-isopropyl-4-methylcyclohexene b) 3-butyl-2-heptene c) 4-methyl-1,2- hexadiene d) trans-3,3-dimethyl-4-propyl-1,5-octadiene e) (42)-2,4-diethyl-1,4-hexadiene f) 1.2-propadiene g) (32,5E) -2,6-dimethyl-1,3,5,7-octatetraene h) cis-2,2,5,5-tetramethyl-3-hexene i) Methylenecyclohexane, j) trans- 1,2 divinylcyclohexane
please answer d e f g
For each of the following structures: (a) Give the IUPAC name. (b) Identify the leaving group. (c) Identify the degree of substitution of the carbon bearing the leaving group. (d) Identify the same carbon as (R) or (S), if applicable. (e) Give the product(s), if any of reaction with NaOH and with NaOCH3- (1) Identify the same carbon as in (c) and (d) in the product as (R) or (S), if applicable. (g) Choose...
PLEASE HELP WITH ALL QUESTIONS
QUESTION 1 1.1 Draw a fully-labelled diagram showing the process of conjugation in Spirogyra. (10) 1.2 List FOUR advantages and FOUR disadvantages of algae. (8) 1.3 Name the different terrestrial biomes of the world and give one diagnostic characteristic of each biome. (12) [30] QUESTION 2 2.1 By means of a labelled diagram, describe the life cycle of an angiosperm. Use blocks of information to explain each stage. (15) 2.2 What are the advantages and...
1Ozonolysis of alkenes yields Alcohol carboxylic acid b-ketones if one of the unsaturated carbon atoms is disubstituted d- alkane 23-Aldehyde C-0 is more polarized than ketone C-O because a-As in carbocations, more alkyl groups stabilize + character b-Ketone has more alkyl groups, stabilizing the C-O carbon inductively c- due to a andb d- none of the above 24-Aldehydes and unhindered ketones react with HCN to form a-Cyanohydrine b-alcohol c- alkyne d- alkene 25-addition of a Grignard reagent to formaldehyde followed...
Examine structures E through H below to answer questions three and four. Onlar onlarowa 3) All four of the structures (E through H) above are insoluble in water. Which of the structures would you expect to become more soluble in water when combined with HCl(aq), and WHY? 4) Which of the structures (E through H) above would you expect to form a salt when mixed with - aqueous sodium hydroxide, and WHY?
as A Questions 1-4 refers to the five titration curves (labelled mL of titrant mL of titrant ml of titrant mL of titrant mL of titrant 1 Which curve shows the titration of a strong acid with a strong base? AA BB CC DD EE Fnone of the above 2 Which curve shows the titration of a weak acid with a strong base? A A BB CC DD EE Fnone of the above 3 Which curve shows the titration of...
write condensed structures fore each of the following
compounds
Homework Problems 7.1 Write condensed structures for each of the following compounds: a. 2,2,4-trimethylpentane b. 5-isopropyl-2-methyloctane c. 1,1,3,3-tetrabromopropane d. 1,1-dichlorocyclopentane e. 1,4-diethylcyclohexane f. 1-bromo-2-methylcyclobutane What are the IUPAC names of the following compounds? 7.2 CH2CH, CH3 a) CH, C CH, CH, CH СH,CH, сн, CH2CH, b) CH2CH d) (CH),CCH2CH e) F Br Br Write the structural formulas and names for FOUR isomers of cycloalkane, CSH10. 7.3 7.4 Propose structures for molecules...
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
Draw correct. condens Cyclic portions of structures condensed structures for the following compounds according to IUPAC rules portions of structures can be done as line-angle drawings (20 pts.) b) |-ethyl-2-methylcyclohexane a) 1.1.2-trichloro-2-fluoropropane d) cis-4,4,5,5-tetramethyl-2-hexene 3-ethyl-2,2,3-trimethyloctane 3,3-dimethyl-1-octyne 4-ethyl-2-heptene 8) 1-chloro-2-propyleyelopropane h) 1,2,4-tribromo-3-chlorocyclohexane i) trans-4-ethyl-2-octene i) 1-bromo-1-chlorocycloheptane 3) hake 1-bromopentane as the only product from the reaction of 1-pentene with Can you easily make 1-bromopentane as the HBr and why? (Explain!) (10 pts.) (HINT: You may want to draw out a chemical...
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