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i know the correct answer is B (pictured below) but can
aomeone explain why Br connected...
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...
Complete the following with the correct products, label Zaitsev and Hofmann, and explain why the reaction...
Complete the following with the correct products, label Zaitsev and Hofmann, and explain why the reaction is either regioselective or stereoselective. (6 pts.) D -Br Nahi Complete each of the following reactions by adding the starting material, reaction conditions, or all possible product(s) - label major/minor - Sx2. Sx1, E2 or E1. (33 pts.) (CH3),COK DMF C(CH3) NaOH DMSO CH OH heat Ph H+Br NaOCH, H+CHE Ph DMF SK DMF o (only product)
how do i know which Hydrogens i affect? what do i do here? can someone explain...
how do i know which Hydrogens i affect? what do i do here? can
someone explain what im supposed to be looking for with drawings
too? i thought this was an aldol condensation but this says its a
michael reaction and the answer is C. thank you so much!
290. Predict the product: CH2=CH-C + OH CH=CH-C°. CH-&-CH2-8-CzHs Hot H2O H O=0 -C-C-C2H5 о но No reaction: base is too weak to allow deprontonation. CH2 e) C2H5-C-C-C-C2H5 CH2 HG он...
unsure why this is wrong where I put my arrows. please explain Consider the El reaction...
unsure why this is wrong where I put my arrows. please
explain
Consider the El reaction of the tertiary halide shown. H Н. .Н OH H :Br: Br: NaOH H product Step 1: Add curved arrow(s). Step 2: Add curved arrow(s). Select More Erase Draw Rings More Erase Select Draw Rings C Br H C н Br re Ts e13
short answer help plz! check the ones i answered and help with the ones i didnt!!...
short answer help plz! check the ones i answered and help with the
ones i didnt!!
9. For the following reaction, what will be the effect on the rate if [NaCN) is halved? 11. Which of these Newman Projections shows the preferred conformation for an E2 reaction to occur? NaCN - Br DMSO product / V I (a) The rate doubles / CH3 (b) The rate triples The rate will be halved (d) The rate stays the same (e) There...
21) Provide the correct product(ss) for the reactionn conditions shown below. If no reaction will occur,...
21) Provide the correct product(ss) for the reactionn conditions shown below. If no reaction will occur, state "no reaction" and briefly explain why for full credit. For products that have stereochemistry clearly show it where necessary. (4 points each; 20 points total) КОН B) Br Н-о NaOC(CH3) D) Br CH3OH NaC Он
ALSO DRAW THE MECHANISM FOR THE CORRECTED 3B 3. The reactions below would not go as planned. Br NaoEt i. Explain why t...
ALSO DRAW THE MECHANISM FOR THE CORRECTED 3B
3. The reactions below would not go as planned. Br NaoEt i. Explain why the reaction did not go as planned. ii. What product would form? iii. How would you change the substrate or the reagent to produce the correct product? 1. LIN(IPP) 2.B part + LIBr + HN/IPr)2 i. Explain why the reaction did not go as planned. ii. What product would form? ill. How would you change the substrate or...
need help on last hw problems, please explain and the answers thank you 6. Draw a...
need help on last hw problems, please explain and the answers thank
you
6. Draw a structural formula for the major organic product of the reaction shown below. (CH2=CHCMa CuLi 7. Draw a structural formula for the major organic product of the reaction shown below. CuLi Draw structural formulas for organic products A and B. 8. Hао Mg В A H3CC=CH2 ether Br 1. Specify whether the tramsformation shown involves net oxidation of carbon, net reduction of carbon, or neither...
Explain why answers are correct. I already know the correct answer, i need to know why....
Explain why answers are correct. I already know the correct
answer, i need to know why.
Figure TXA. Suppose the government imposes a $10 per-unit tax on a good. 20+ A - - 16+ 14+ 12+- - - - FI 10+ D il H G -- - -- -- - 4+ K L ; M - - - 4 8 12 16 20 24 28 32 36 0 17. See Figure TXA. The tax causes consumer surplus to decrease by...
Please answer 29 and explain. Thank you Where would the compound shown undergo monobromination wiuh Br/FeBrs...
Please answer 29 and explain. Thank you
Where would the compound shown undergo monobromination wiuh Br/FeBrs (2 points)? Why (4 points)? A. ortho/para positions on ring 1 0 B. meta position on ring 1 D. meta position on ring 2 ring 1 nin2 C. ortho/para positions on ring 2 E. mixture of meta position on ring 1 and ortho/para positions on ring 2 Which of the following compounds has the fastest SN1 reaction rate with H-O in acetone (2 pe?...
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...
Complete the following with the correct products, label Zaitsev and Hofmann, and explain why the reaction is either regioselective or stereoselective. (6 pts.) D -Br Nahi Complete each of the following reactions by adding the starting material, reaction conditions, or all possible product(s) - label major/minor - Sx2. Sx1, E2 or E1. (33 pts.) (CH3),COK DMF C(CH3) NaOH DMSO CH OH heat Ph H+Br NaOCH, H+CHE Ph DMF SK DMF o (only product)
how do i know which Hydrogens i affect? what do i do here? can
someone explain what im supposed to be looking for with drawings
too? i thought this was an aldol condensation but this says its a
michael reaction and the answer is C. thank you so much!
290. Predict the product: CH2=CH-C + OH CH=CH-C°. CH-&-CH2-8-CzHs Hot H2O H O=0 -C-C-C2H5 о но No reaction: base is too weak to allow deprontonation. CH2 e) C2H5-C-C-C-C2H5 CH2 HG он...
unsure why this is wrong where I put my arrows. please
explain
Consider the El reaction of the tertiary halide shown. H Н. .Н OH H :Br: Br: NaOH H product Step 1: Add curved arrow(s). Step 2: Add curved arrow(s). Select More Erase Draw Rings More Erase Select Draw Rings C Br H C н Br re Ts e13
short answer help plz! check the ones i answered and help with the
ones i didnt!!
9. For the following reaction, what will be the effect on the rate if [NaCN) is halved? 11. Which of these Newman Projections shows the preferred conformation for an E2 reaction to occur? NaCN - Br DMSO product / V I (a) The rate doubles / CH3 (b) The rate triples The rate will be halved (d) The rate stays the same (e) There...
21) Provide the correct product(ss) for the reactionn conditions shown below. If no reaction will occur, state "no reaction" and briefly explain why for full credit. For products that have stereochemistry clearly show it where necessary. (4 points each; 20 points total) КОН B) Br Н-о NaOC(CH3) D) Br CH3OH NaC Он
ALSO DRAW THE MECHANISM FOR THE CORRECTED 3B
3. The reactions below would not go as planned. Br NaoEt i. Explain why the reaction did not go as planned. ii. What product would form? iii. How would you change the substrate or the reagent to produce the correct product? 1. LIN(IPP) 2.B part + LIBr + HN/IPr)2 i. Explain why the reaction did not go as planned. ii. What product would form? ill. How would you change the substrate or...
need help on last hw problems, please explain and the answers thank
you
6. Draw a structural formula for the major organic product of the reaction shown below. (CH2=CHCMa CuLi 7. Draw a structural formula for the major organic product of the reaction shown below. CuLi Draw structural formulas for organic products A and B. 8. Hао Mg В A H3CC=CH2 ether Br 1. Specify whether the tramsformation shown involves net oxidation of carbon, net reduction of carbon, or neither...
Explain why answers are correct. I already know the correct
answer, i need to know why.
Figure TXA. Suppose the government imposes a $10 per-unit tax on a good. 20+ A - - 16+ 14+ 12+- - - - FI 10+ D il H G -- - -- -- - 4+ K L ; M - - - 4 8 12 16 20 24 28 32 36 0 17. See Figure TXA. The tax causes consumer surplus to decrease by...
Please answer 29 and explain. Thank you
Where would the compound shown undergo monobromination wiuh Br/FeBrs (2 points)? Why (4 points)? A. ortho/para positions on ring 1 0 B. meta position on ring 1 D. meta position on ring 2 ring 1 nin2 C. ortho/para positions on ring 2 E. mixture of meta position on ring 1 and ortho/para positions on ring 2 Which of the following compounds has the fastest SN1 reaction rate with H-O in acetone (2 pe?...
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