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all 3 questions please. thank you in advance!!
Question 8: Draw the Syl and El products...
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
for f - j draw structures pls help with #1 as well f) 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen...
for f - j draw structures pls help with #1 as well
f) 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen h) E-5-bromo-4-chloro-7,7-dimethyl-4-undecene i) Z-1,2-difluoro-cyclohexene i) 4-ethenylcyclohexano Predict the major organic product or products of each of the following reactions. a) (CH3),CHCH-CH: H2SO4 HO b) (CH3),CHCH-CH, 1. Hg(OAc), H20 2. NaBH4 1. BH-THF c) (CH3),CHCH-CH2 2. H,O, NaOH
3 & 4 please Draw all possible El elimination products and indicate which alkene is the...
3
& 4 please
Draw all possible El elimination products and indicate which alkene is the major product: CH3OH CH3 a) HC-C-ci CH3 CH3CH2OH CH3C430H CH3CH2OH Br CH3CH2OH I X ORSOGON CH3OH Br brow all possible E2 elimination products and indicate which okene is the major product CH, ON CH, OH CHÚCHONa CH,CH OH CHÚCH ONa CH,CH, OH CH3CH2ONa d YoX CH₂CH₂OH CH,CH OH (CH3),COH TONE CH,(CH)CH,OH CHCH,ONa CH,CH,OH CH,CH, CH,CH,ONa CH,CH, OH CH,
Please answer number 2 and 3 completely , thank you CH3 он н* CH3 нус"Гон, -...
Please answer number 2 and 3 completely , thank you
CH3 он н* CH3 нус"Гон, - H2O CH3 Hacito CH3 СР НАС нс H₂ cuota нс сн, H5C Figure 1 Conversion of t-butanol into t-butyl chloride by an Syl mechanism 1. Write the mechanism for the reaction in this experiment showing the flow of electrons. w friends are Jo carbuention arty worth eny - 2. What is the theoretical yield of the product in this reaction? Write this down and...
1. Draw all of the constitutional isomers that are formed in each elimination reaction and label...
1. Draw all of the constitutional isomers that are formed in each elimination reaction and label the mechanism as E2 or E1. a. 2-bromo butane reacts with methoxide b. 1-chloro-1-ethyl 2 methyl cyclopentane reacts with water 2. For which reaction mechanism are each of the following statements true? Mechanism S1, S2, E1 or E2. A statement may be true for one or more mechanisms a. The mechanism involves carbocation intermediates b. The mechanism has two steps C. The reaction rate...
Please Answer these Organic Chemistry questions. Thank you. ド 3. a. Draw the 3D structures of...
Please Answer these Organic Chemistry questions.
Thank you.
ド 3. a. Draw the 3D structures of the stero isomers of 2-bromo-3-chlorobutane. Mention their configuration and the relation between them. b. As a but for 1,2-diethylcyclopentane. 4. a. React 1-butanol with HBr, and 2-methyl-2-butanol with HCI. Write the R.D.S step in the mechanism of each reaction. b. Draw the products of S reaction of (S)-2-butanol with HCl using TsCl. Similarly CH,OK with (R)-3-bromo-3-methylhexane Do 5. a. Write the products and mechanism...
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 ANSWER ALL QUESTIONS Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms....
PLEASE ANSWER ALL QUESTIONS
Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms. The question only requires you to address the E2 reaction only. For the E2 reaction: Use Newman projections to show the relationship between the leaving group and the beta-hydrogen on the carbon labeled with the asterisk ("). 1. If the leaving group and the beta-hydrogen on the carbon labeled with the asterisk (1) are not in the correct orientation, show the result of the...
can you please show the reaction for a couple parts of each question? 3. Draw the...
can you please show the reaction for a couple parts of each
question?
3. Draw the structure(s) of the alkynes formed when the following are reacted with a strong base such as potassium hydroxide or sodium amide. CH ci CH,CHCIK CH3CH2CCHCH BY CH3CCH,CHE CHCH C H3CHCHCH3 CH3CCHE . нус Br Br f. Ci CI (CH3)2CHCHCH2BE (CH3)3CCCHg g. Br h. Ci 4. Draw the structure of the dihalide that could be used to prepare each alkyne shown using a strong base....
please help me with questions from 3-10! and the bonus. thank you so much Directions: Place...
please help me with questions from 3-10! and the bonus.
thank you so much
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CU CECH A. B sp,sp? sp, sp sp, sp sp', sp sp, sp Ans. 2. What is the IUPAC name for the molecule shown below? os B. C. D. E. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne...
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
for f - j draw structures pls help with #1 as well
f) 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen h) E-5-bromo-4-chloro-7,7-dimethyl-4-undecene i) Z-1,2-difluoro-cyclohexene i) 4-ethenylcyclohexano Predict the major organic product or products of each of the following reactions. a) (CH3),CHCH-CH: H2SO4 HO b) (CH3),CHCH-CH, 1. Hg(OAc), H20 2. NaBH4 1. BH-THF c) (CH3),CHCH-CH2 2. H,O, NaOH
3
& 4 please
Draw all possible El elimination products and indicate which alkene is the major product: CH3OH CH3 a) HC-C-ci CH3 CH3CH2OH CH3C430H CH3CH2OH Br CH3CH2OH I X ORSOGON CH3OH Br brow all possible E2 elimination products and indicate which okene is the major product CH, ON CH, OH CHÚCHONa CH,CH OH CHÚCH ONa CH,CH, OH CH3CH2ONa d YoX CH₂CH₂OH CH,CH OH (CH3),COH TONE CH,(CH)CH,OH CHCH,ONa CH,CH,OH CH,CH, CH,CH,ONa CH,CH, OH CH,
Please answer number 2 and 3 completely , thank you
CH3 он н* CH3 нус"Гон, - H2O CH3 Hacito CH3 СР НАС нс H₂ cuota нс сн, H5C Figure 1 Conversion of t-butanol into t-butyl chloride by an Syl mechanism 1. Write the mechanism for the reaction in this experiment showing the flow of electrons. w friends are Jo carbuention arty worth eny - 2. What is the theoretical yield of the product in this reaction? Write this down and...
1. Draw all of the constitutional isomers that are formed in each elimination reaction and label the mechanism as E2 or E1. a. 2-bromo butane reacts with methoxide b. 1-chloro-1-ethyl 2 methyl cyclopentane reacts with water 2. For which reaction mechanism are each of the following statements true? Mechanism S1, S2, E1 or E2. A statement may be true for one or more mechanisms a. The mechanism involves carbocation intermediates b. The mechanism has two steps C. The reaction rate...
Please Answer these Organic Chemistry questions.
Thank you.
ド 3. a. Draw the 3D structures of the stero isomers of 2-bromo-3-chlorobutane. Mention their configuration and the relation between them. b. As a but for 1,2-diethylcyclopentane. 4. a. React 1-butanol with HBr, and 2-methyl-2-butanol with HCI. Write the R.D.S step in the mechanism of each reaction. b. Draw the products of S reaction of (S)-2-butanol with HCl using TsCl. Similarly CH,OK with (R)-3-bromo-3-methylhexane Do 5. a. Write the products and mechanism...
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 ANSWER ALL QUESTIONS
Question 5 The reaction below occurs via SN2 and E2 reaction mechanisms. The question only requires you to address the E2 reaction only. For the E2 reaction: Use Newman projections to show the relationship between the leaving group and the beta-hydrogen on the carbon labeled with the asterisk ("). 1. If the leaving group and the beta-hydrogen on the carbon labeled with the asterisk (1) are not in the correct orientation, show the result of the...
can you please show the reaction for a couple parts of each
question?
3. Draw the structure(s) of the alkynes formed when the following are reacted with a strong base such as potassium hydroxide or sodium amide. CH ci CH,CHCIK CH3CH2CCHCH BY CH3CCH,CHE CHCH C H3CHCHCH3 CH3CCHE . нус Br Br f. Ci CI (CH3)2CHCHCH2BE (CH3)3CCCHg g. Br h. Ci 4. Draw the structure of the dihalide that could be used to prepare each alkyne shown using a strong base....
please help me with questions from 3-10! and the bonus.
thank you so much
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CU CECH A. B sp,sp? sp, sp sp, sp sp', sp sp, sp Ans. 2. What is the IUPAC name for the molecule shown below? os B. C. D. E. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne...
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