Homework Answers
NBS is a selective brominating reagent at allylic and Benzyl position.
Na/ NH3 is Birch reduction and reduce the benzene ring to diene.
Na2Cr2O7 is a strong oxidizing agent responsible for oxidation of benzyl carbon to COOH.
Hydroboration oxidation by Anti-markonikoff addition.
Diels Alder reaction of anthracene and maleic anhydride gives the following adduct.
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Least reactive Most reactive 12.53)...
the answers i circled are incorrect. can you give me the correct answers and explain why?...
the answers i circled are incorrect. can you give me the
correct answers and explain why?
For each structure. (1) starany asymmetric carbon atom cture as chilor achiraland (4) label any mes structure (2) label enchan asymmetric carbon as Ros tre cabos ) label the CH3 н H- — Br OH Chiral ₂ CH₂Br oH f Br achiral @ CH Bro 24) Give the solvolysis product expected when each compound is heated in ethanol. 25) Predict the reaction product CHCH...
CH3 (4) 1. Which of the following alkyl halides would you expect to be most reactive...
CH3 (4) 1. Which of the following alkyl halides would you expect to be most reactive in a unimolecular reaction? a) C&H, CH, CH, CH, BY b) CH 1 CH CH Br C) CH11CCH, Br d) C6H CH2 CH CHỊ CHỊ CH3 CHỊ e) C&H, CCH Br CHE (4) 2. What would you expect to be the chief organic product(s) when tert-butyl bromide reacts with sodium acetylide, i.e., CH3 + - CH2-C-Br + Na :CECH — ? CH a) I...
1. (10 points) la. Rank the following substrates from most (1) to least reactive (4) in...
1. (10 points) la. Rank the following substrates from most (1) to least reactive (4) in an SN2 reaction. Explain the reason for your choice Br ABT Chrobr 1b. Rank the following substrates from most (1) to least reactive (3) in an SNI reaction. Explain the reason for your choice lc. What is the nucleophile in the following reaction? ~ Br + CHỌCoona - OOCCH3 OOCCH + M NaBr 1d. What is the electrophile in the following reaction? Br +...
() 1. Which of the following alkyl holides would you expect to be most reactive in a unimolecular reaction? CH3 a)...
() 1. Which of the following alkyl holides would you expect to be most reactive in a unimolecular reaction? CH3 a) CsM , CH, CH, CH, Br b) CEHCH CH BY c) CH, CCH, Br d) CH, CH2 CH CHE сн. он сня Br e) CHICCHE CH3 (4). 2. What would you expect to be the chief organic product(s) when tert-butyl bromide reacts with sodium acetylide, i.e.. CH + - CH3-C-Br + Na CECH ? CH a) 1 b) II...
multiple choise 5 questions answer all please 1.Which of the following compounds is the least reactive...
multiple choise 5 questions answer all please 1.Which of the following compounds is the least reactive in the nucleophilic substitution with NaOH? 2,4-dinitrochlorobenzene m-nitrochlorobenzene o-nitrochlorobenzene 3,5-dinitrochlorobenzene 2.which of the following is the correct ascending order, for boiling points? a. n-butane <1-butane <diethyl ether <2-butanone b. n-butane <2-butanone <diethyl ether <1-butane c. n-butane <diethyl ether <1-butane <2-butanone d. n-butane <diethyl ether <2-butanone <1-butane 3.What is the main product of the reaction between 1-cyclobutyl-1-ethanol and H2SO4 + heat? a. 1-methyl cyclopentene b....
please help!! thank you! Which of the following compounds is most reactive towards nucleophilic addition reaction?...
please help!! thank you!
Which of the following compounds is most reactive towards nucleophilic addition reaction? H1 H H A B С D E Predict the product for the following reaction sequence. iii PBrz Mg/ether Н H Cr04 ОН 2. Hz0+ A. 6,7-dimethyl-3-nonanol B. 6,7-dimethyl-3-nonanone C. 6,7-dimethyl-3-nonanal D. 3,4-dimethyl-7-nonanol E. 3,4-dimethyl-7-nonanone Predict the product for the following reaction 1. LiAlH4 (excess) 2. H30* OH OH OH -Н HO B с D Provide the structure of the ylide needed to prepare...
Please give detailed answers to the pre and post lab questions. Thank you! NUCLEOPHILIC DISPLACEMENT- FORMATION...
Please give detailed answers to the pre and post lab questions.
Thank you!
NUCLEOPHILIC DISPLACEMENT- FORMATION OF AN ETHER BY AN SN2 REACTION Bond formation by use of an SN2 reaction is very important for organic and biological synthesis. Many new bonds formed make use of this versatile reaction pathway. In this reaction, one partner is the nucleophile and the other partner is the electrophile. The electrophile will have a leaving group that will be lost in the reaction. In...
all 3 questions please. thank you in advance!! Question 8: Draw the Syl and El products...
all 3 questions please. thank you in advance!!
Question 8: Draw the Syl and El products formed in the reaction of (CH3)3CBr with H,0. Show mechanism using arrows." CH3 CH3-C-Br + CH H-O-H Question 9: Draw the major E2 elimination product formed from the following: alkyl halide. Question 10: Give structures corresponding to each name. a)-7,7-dimethyl-4-octanol b)>5-methyl-4-propyl-3-heptanol" c)-2-tert-butyl-3-methylcyclohexanolº d)- trans-1,2-cyclohexanediol"
plz answer all multiple choice questions fastttttt and thank youuu art (10) Answer at least 6...
plz answer all multiple choice questions
fastttttt and thank youuu
art (10) Answer at least 6 of the following 10 questions. You may answer extra questions, but a 2 point deduction will be asso ich extra incorrect answer. For those questions marked with an asterisk, a correct rank will earn you a 5 point bons. If you don't kn structure that is named you may buy it for a lpt deduction For questions marked with a sign a 3 point...
the answers i circled are incorrect except for 13. i know 11 is d and 15 is a. can you please explain why these three a...
the answers i circled are incorrect except for 13. i know 11
is d and 15 is a. can you please explain why these three are
correct as well. can you give me the correct answers and explain
why?
de motor and h ow w generation recognized disorder that can benefit from hippothy wy b o cice to which they were anached indiactive donation of electron density to the cationic center chan inductive removal of electron density from the w...
the answers i circled are incorrect. can you give me the
correct answers and explain why?
For each structure. (1) starany asymmetric carbon atom cture as chilor achiraland (4) label any mes structure (2) label enchan asymmetric carbon as Ros tre cabos ) label the CH3 н H- — Br OH Chiral ₂ CH₂Br oH f Br achiral @ CH Bro 24) Give the solvolysis product expected when each compound is heated in ethanol. 25) Predict the reaction product CHCH...
CH3 (4) 1. Which of the following alkyl halides would you expect to be most reactive in a unimolecular reaction? a) C&H, CH, CH, CH, BY b) CH 1 CH CH Br C) CH11CCH, Br d) C6H CH2 CH CHỊ CHỊ CH3 CHỊ e) C&H, CCH Br CHE (4) 2. What would you expect to be the chief organic product(s) when tert-butyl bromide reacts with sodium acetylide, i.e., CH3 + - CH2-C-Br + Na :CECH — ? CH a) I...
1. (10 points) la. Rank the following substrates from most (1) to least reactive (4) in an SN2 reaction. Explain the reason for your choice Br ABT Chrobr 1b. Rank the following substrates from most (1) to least reactive (3) in an SNI reaction. Explain the reason for your choice lc. What is the nucleophile in the following reaction? ~ Br + CHỌCoona - OOCCH3 OOCCH + M NaBr 1d. What is the electrophile in the following reaction? Br +...
() 1. Which of the following alkyl holides would you expect to be most reactive in a unimolecular reaction? CH3 a) CsM , CH, CH, CH, Br b) CEHCH CH BY c) CH, CCH, Br d) CH, CH2 CH CHE сн. он сня Br e) CHICCHE CH3 (4). 2. What would you expect to be the chief organic product(s) when tert-butyl bromide reacts with sodium acetylide, i.e.. CH + - CH3-C-Br + Na CECH ? CH a) 1 b) II...
please help!! thank you!
Which of the following compounds is most reactive towards nucleophilic addition reaction? H1 H H A B С D E Predict the product for the following reaction sequence. iii PBrz Mg/ether Н H Cr04 ОН 2. Hz0+ A. 6,7-dimethyl-3-nonanol B. 6,7-dimethyl-3-nonanone C. 6,7-dimethyl-3-nonanal D. 3,4-dimethyl-7-nonanol E. 3,4-dimethyl-7-nonanone Predict the product for the following reaction 1. LiAlH4 (excess) 2. H30* OH OH OH -Н HO B с D Provide the structure of the ylide needed to prepare...
Please give detailed answers to the pre and post lab questions.
Thank you!
NUCLEOPHILIC DISPLACEMENT- FORMATION OF AN ETHER BY AN SN2 REACTION Bond formation by use of an SN2 reaction is very important for organic and biological synthesis. Many new bonds formed make use of this versatile reaction pathway. In this reaction, one partner is the nucleophile and the other partner is the electrophile. The electrophile will have a leaving group that will be lost in the reaction. In...
all 3 questions please. thank you in advance!!
Question 8: Draw the Syl and El products formed in the reaction of (CH3)3CBr with H,0. Show mechanism using arrows." CH3 CH3-C-Br + CH H-O-H Question 9: Draw the major E2 elimination product formed from the following: alkyl halide. Question 10: Give structures corresponding to each name. a)-7,7-dimethyl-4-octanol b)>5-methyl-4-propyl-3-heptanol" c)-2-tert-butyl-3-methylcyclohexanolº d)- trans-1,2-cyclohexanediol"
plz answer all multiple choice questions
fastttttt and thank youuu
art (10) Answer at least 6 of the following 10 questions. You may answer extra questions, but a 2 point deduction will be asso ich extra incorrect answer. For those questions marked with an asterisk, a correct rank will earn you a 5 point bons. If you don't kn structure that is named you may buy it for a lpt deduction For questions marked with a sign a 3 point...
the answers i circled are incorrect except for 13. i know 11
is d and 15 is a. can you please explain why these three are
correct as well. can you give me the correct answers and explain
why?
de motor and h ow w generation recognized disorder that can benefit from hippothy wy b o cice to which they were anached indiactive donation of electron density to the cationic center chan inductive removal of electron density from the w...
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