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can you please show the reaction for a couple parts of each
question?
3. Draw the...
Quickly show all steps and answers all parts of the question please thank you 2. Show...
Quickly show all steps and answers all parts of the question
please thank you
2. Show the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CH3 OH conc. HBO CH₂ H₂CX Br CH₂ H3C CHE H₃C CH Swi condition Br L CH3 CH3 H₃C HC X X
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 help with question 5 part b and show work. thank you!! Draw the curved arrows...
please help with question 5 part b and show work. thank
you!!
Draw the curved arrows that accomplish the following transformation: CH HC нс H -CH₂ H-O CH H H.C Closs of a leaving group) Question 5: Predict whether the following carbocation will rearrange, and if so, draw the curved arrow showing the carbocation rearrangement: a) I C-CH₂ сн. I I No rearrangement blc it is already I cancration, which is more stable than I carbocation, b) CH3 CH, CH...
please be clear in drawings to show where areas are coming from and what theyre pointing...
please be clear in drawings to show where areas are coming from and
what theyre pointing to
[Review Topical [References] Electrophilic addition of bromine, Bry, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH CI, In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due...
1. Calculate AH for each reaction using bond dissociation values. Determine if the reaction is exothermic...
1. Calculate AH for each reaction using bond dissociation values. Determine if the reaction is exothermic or endothermic a. CH3CH2CH3 + Br2 — CHșCH,CH,-Br + HBr ОН + H₂O + HI 498 297 aaa 720 - 698 - 22 401 andiotamie Table 6.2 Bond Dissociation Energies for Some Common Bonds IA-B - A. + .B] Bond AH kJ/mol (kcal/mol) Bond AH kJ/mol kcal/mol) 456 569 431 H-Z bonds H-F H-CI H-Br H-1 Н-ОН (136) (103) (88) 368 297 498 (71)...
9.13 Draw a structural formula for the product of each S 2 reaction. Where configuration of...
9.13 Draw a structural formula for the product of each S 2 reaction. Where configuration of the starting material is given, show the configuration of the product. (a) CH,CH,CH,Cl + CH,CH,O-Nat - (b) (CH3)3N + CHI acetone (c) CHBr + Na*CN- acetone CI + CH2S+Na+ - (d) HC ethanol (e) CHỊCH,CH,Cl + CHỤC=C Li* ( -chĄC + NH; echanol diethyl ether (g) 0 NH + CH3(CHỊ) CHỊC14 (h) CH CH.CH,Br + NaCN to acetone 9.16 Treatment of 1-aminoadamantane, CH, N,...
please help with both parts of question number one. thanks! 1. For each reaction below, draw...
please help with both parts of question number one.
thanks!
1. For each reaction below, draw the reaction mechanism for the rate determining step. On the starting structures, draw all appropriate arrows to indicate the flow of electrons. Fill in the box above the arrows with the reaction mechanism as SN1 or SN2. Draw the first key transition state product(s). Use dotted lines to indicate bonds that are in the process of being broken or made. Write all formal charges....
Please include complete answers only, thank you. a. Draw the structural formula of each of the...
Please include complete answers only, thank you.
a. Draw the structural formula of each of the following compounds. b. According to the character of the bold, enlarged carbon(s) label each compound "basic", "electrophilic" or "nucleophilic". c. Diagram electron pushing (resonance), and inductive effects d. Give a brief narrative (one or two short sentences) to explain what your diagrams show regarding your choice (base, electrophile, or nucleophile): 16% (2% each) (CH3)2N=C(CH3)2CI (CH3)2C=CHCH=CHN(CH3)2 CH2=CH(OH) H(C=NH)CH=CH2 CH2=CHCHENH KCH3CH(C=O)CH3 CH3CH2(C=O)Br CH3CH2(C=O)H
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"
Can someone help with question 2 and 3 please? I already asked for question 2 two...
Can someone help with question 2 and 3 please? I already asked
for question 2 two times but i got wrong answers i just need the
products for each one. Thanks
Demogud 2o chloro ethyl-4-methyl Pentanoate 2. Draw a structure for each of the following named compounds: a) ($)-2-amino-3-hydroxypropanoic acid. a) NAVAH HON b) ethyl 2,3-dimethyl-2-butenoate 22 cooH BI C O-CH-CH2 3. Predict the products for the following reactions: SOCI pyridine OH 1) LDA, -78°C НС. CH3 2) CH CHCH,...
Quickly show all steps and answers all parts of the question
please thank you
2. Show the step by step mechanism to account for the following transformation. Also predict the major product formed. (20 points) CH3 OH conc. HBO CH₂ H₂CX Br CH₂ H3C CHE H₃C CH Swi condition Br L CH3 CH3 H₃C HC X X
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 help with question 5 part b and show work. thank
you!!
Draw the curved arrows that accomplish the following transformation: CH HC нс H -CH₂ H-O CH H H.C Closs of a leaving group) Question 5: Predict whether the following carbocation will rearrange, and if so, draw the curved arrow showing the carbocation rearrangement: a) I C-CH₂ сн. I I No rearrangement blc it is already I cancration, which is more stable than I carbocation, b) CH3 CH, CH...
please be clear in drawings to show where areas are coming from and
what theyre pointing to
[Review Topical [References] Electrophilic addition of bromine, Bry, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH CI, In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due...
1. Calculate AH for each reaction using bond dissociation values. Determine if the reaction is exothermic or endothermic a. CH3CH2CH3 + Br2 — CHșCH,CH,-Br + HBr ОН + H₂O + HI 498 297 aaa 720 - 698 - 22 401 andiotamie Table 6.2 Bond Dissociation Energies for Some Common Bonds IA-B - A. + .B] Bond AH kJ/mol (kcal/mol) Bond AH kJ/mol kcal/mol) 456 569 431 H-Z bonds H-F H-CI H-Br H-1 Н-ОН (136) (103) (88) 368 297 498 (71)...
9.13 Draw a structural formula for the product of each S 2 reaction. Where configuration of the starting material is given, show the configuration of the product. (a) CH,CH,CH,Cl + CH,CH,O-Nat - (b) (CH3)3N + CHI acetone (c) CHBr + Na*CN- acetone CI + CH2S+Na+ - (d) HC ethanol (e) CHỊCH,CH,Cl + CHỤC=C Li* ( -chĄC + NH; echanol diethyl ether (g) 0 NH + CH3(CHỊ) CHỊC14 (h) CH CH.CH,Br + NaCN to acetone 9.16 Treatment of 1-aminoadamantane, CH, N,...
please help with both parts of question number one.
thanks!
1. For each reaction below, draw the reaction mechanism for the rate determining step. On the starting structures, draw all appropriate arrows to indicate the flow of electrons. Fill in the box above the arrows with the reaction mechanism as SN1 or SN2. Draw the first key transition state product(s). Use dotted lines to indicate bonds that are in the process of being broken or made. Write all formal charges....
Please include complete answers only, thank you.
a. Draw the structural formula of each of the following compounds. b. According to the character of the bold, enlarged carbon(s) label each compound "basic", "electrophilic" or "nucleophilic". c. Diagram electron pushing (resonance), and inductive effects d. Give a brief narrative (one or two short sentences) to explain what your diagrams show regarding your choice (base, electrophile, or nucleophile): 16% (2% each) (CH3)2N=C(CH3)2CI (CH3)2C=CHCH=CHN(CH3)2 CH2=CH(OH) H(C=NH)CH=CH2 CH2=CHCHENH KCH3CH(C=O)CH3 CH3CH2(C=O)Br CH3CH2(C=O)H
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"
Can someone help with question 2 and 3 please? I already asked
for question 2 two times but i got wrong answers i just need the
products for each one. Thanks
Demogud 2o chloro ethyl-4-methyl Pentanoate 2. Draw a structure for each of the following named compounds: a) ($)-2-amino-3-hydroxypropanoic acid. a) NAVAH HON b) ethyl 2,3-dimethyl-2-butenoate 22 cooH BI C O-CH-CH2 3. Predict the products for the following reactions: SOCI pyridine OH 1) LDA, -78°C НС. CH3 2) CH CHCH,...
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