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3 & 4 please write it neat so i can understand
please
3. In the deuterium-labeled...
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following...
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium (D) or not. (20 pts) HC CH, ОН TH 0 H,SO.(aq) heat D HC NaOCH.CH CH2CH,OH heat CH, (ii) Write a detail mechanism for the formation of the product in question 30). 4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts) НО. Dr. Denton
3. In the deuterium-labeled compound below predict the product(s) of the elimination of the following elimination...
3. In the deuterium-labeled compound below predict the product(s) of the elimination of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HAC CH OHH .SO.( heat HCP, H NaOCH.CH CHCHOH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 30. 4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts) 0
3. In the deuterium-labeled compound below predict the product(s) of the elimination of the following elimination...
3. In the deuterium-labeled compound below predict the product(s) of the elimination of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HAC CH OH H,SO (aq) hear o H2CD NaOCH.CH CHCH OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 31. 4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts) HO,
3. In the deuterium labeled compound below nredict the products of the elimination of the following elimination rea...
3. In the deuterium labeled compound below nredict the products of the elimination of the following elimination reaction and tell whether the alkene formed contains deutenum or not. (20 pts) HC CH3 OH H2SO4(aq) IH heat нстр (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(1).
3. In the deuterium -labeled compound below predict the product (s) of the elimination reactions of...
3. In the deuterium -labeled compound below predict the product (s) of the elimination reactions of the following elimination reaction and tell whether the alkene formed contains deuterium (D) or not. (20 pts) Н.с, сн, OH H2SO&(aq) (i) heat НС NAOCH2CH3 (ii) CH3CH2OH н CH3 heat (iii) Write a detail mechanism for the formation of the product in question 3(i)
Quickly show all steps and answers all parts of the question please thank you 3. In...
Quickly show all steps and
answers all parts of the question please thank you
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HCCH; OH H2SO4(aq) heat н,с (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(i).
please show all steps including each mechanism (arrows) and also if SN1 has any rearrangements of...
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
please explain in as much detail as possible so I can understand 2/4 6. Identify the...
please explain in as much detail as possible so I can
understand
2/4 6. Identify the major and minor products for each of the following reactions, considering the base that is used: NaOH (CH3),COK b X CH)COS , ) NaOCH CH; (CH3),COK
can someone please explain how to do this with as much detail as possible. someone tried...
can someone please explain how to do this with as much detail
as possible. someone tried to explain it earlier in relation to
(a,e) and (e,a) but im not sure even what that means
Bccurance of Methyl shift o. The following two elimination reactions are found to have very different rates of reaction. The cis compound produces two products and it reacts much faster than the trans isomer, which produces only one product. Explain these observations (the erence in rate...
please answer all of the following questions. 02 pts.] Briefly explain why the following reaction yields...
please answer all of the following questions.
02 pts.] Briefly explain why the following reaction yields the Hofmann product exclusively even though the base is not sterically hindered: This is breause Br is a jood Ieavng Br CH,CH2ONa oup on q dcarloon. CH,CH,он [02 pts.] Draw the structure of alkyl that will undergo an E2 elimination to yield only the indicated alkene. CHyCHONa CHсH,он [04 pts.] Draw only the major product for each of the following elimination reactions. сн-сH,ON CнH-CHон...
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium (D) or not. (20 pts) HC CH, ОН TH 0 H,SO.(aq) heat D HC NaOCH.CH CH2CH,OH heat CH, (ii) Write a detail mechanism for the formation of the product in question 30). 4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts) НО. Dr. Denton
3. In the deuterium-labeled compound below predict the product(s) of the elimination of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HAC CH OHH .SO.( heat HCP, H NaOCH.CH CHCHOH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 30. 4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts) 0
3. In the deuterium-labeled compound below predict the product(s) of the elimination of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HAC CH OH H,SO (aq) hear o H2CD NaOCH.CH CHCH OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 31. 4. Name the following compounds and state the orientation around the double bond (cis/trans or E/Z) (10 pts) HO,
3. In the deuterium labeled compound below nredict the products of the elimination of the following elimination reaction and tell whether the alkene formed contains deutenum or not. (20 pts) HC CH3 OH H2SO4(aq) IH heat нстр (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(1).
3. In the deuterium -labeled compound below predict the product (s) of the elimination reactions of the following elimination reaction and tell whether the alkene formed contains deuterium (D) or not. (20 pts) Н.с, сн, OH H2SO&(aq) (i) heat НС NAOCH2CH3 (ii) CH3CH2OH н CH3 heat (iii) Write a detail mechanism for the formation of the product in question 3(i)
Quickly show all steps and
answers all parts of the question please thank you
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HCCH; OH H2SO4(aq) heat н,с (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(i).
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
please explain in as much detail as possible so I can
understand
2/4 6. Identify the major and minor products for each of the following reactions, considering the base that is used: NaOH (CH3),COK b X CH)COS , ) NaOCH CH; (CH3),COK
can someone please explain how to do this with as much detail
as possible. someone tried to explain it earlier in relation to
(a,e) and (e,a) but im not sure even what that means
Bccurance of Methyl shift o. The following two elimination reactions are found to have very different rates of reaction. The cis compound produces two products and it reacts much faster than the trans isomer, which produces only one product. Explain these observations (the erence in rate...
please answer all of the following questions.
02 pts.] Briefly explain why the following reaction yields the Hofmann product exclusively even though the base is not sterically hindered: This is breause Br is a jood Ieavng Br CH,CH2ONa oup on q dcarloon. CH,CH,он [02 pts.] Draw the structure of alkyl that will undergo an E2 elimination to yield only the indicated alkene. CHyCHONa CHсH,он [04 pts.] Draw only the major product for each of the following elimination reactions. сн-сH,ON CнH-CHон...
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