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Why the answer is D?
Why choice C and E cannot be an answer? It looks...
1) What is the product of the following aldol addition of two aldehydes reaction Өон CH.CH.CH...
1) What is the product of the following aldol addition of two aldehydes reaction Өон CH.CH.CH сн,сн: снҫнн CH. B) CH:CH.CHCHH сн: Сн, он cң, сн: сненнн СН: D) cң, сн: Снінен CH₃CH: E) он cң, cң сн: Снінен сн: 2) Draw the enone product of the following reaction: HO, HO, 3 HC CH HỌC CH 3) What is the product of the following crossed aldol addition reaction? "ОН CH, CHỊCH + H C H (excess) CH3CH2CHCH IV. CH3CHCH Сн,он...
the weakest base: CH3 HO HS the fastest in an Syl reaction: (CE)_CACHOSCH (CH3CB (CH.) CHCH(Br)CH, (CH),C(Br)CH (CH...
the weakest base: CH3 HO HS the fastest in an Syl reaction: (CE)_CACHOSCH (CH3CB (CH.) CHCH(Br)CH, (CH),C(Br)CH (CH3)2CHCH Br 2. For each pair of reactions given below indicate which is faster and explain your reasoning. + CHỊ N + C CH3Cl + N CH3 + Ng CH₃N₂ + i CHg. + NaCN CH, CN + Nal DMSO CH3-1 + NaCN C H, CN + Nal Cho (c) CH,0 + CH,CH,Br - HƠ + CHỊCH,Br CH,CH,OCH, + Bril CH,CH,OH + Br...
Please explain how you got the answer What are the products implied by the two different...
Please explain how you got the answer
What are the products implied by the two different mechanistic pathways shown here? PATHWAYA CHCH, - PATHWAY B A + B HECH CHCH CH снен TIT [B] A is II: B is! [E] A is III: B is IV [C] A is l; B is III [A] A is II: B is III [D] A is 1. Bis IV Explanation for your choice (4 pts) Which of these "curved arrows" describe a mechanism...
organic chemistry answer is D. Can someone please explain why? 3. Which reaction would proceed the...
organic chemistry
answer is D.
Can someone please explain why?
3. Which reaction would proceed the fastest? (A) CH3CH2OCH2 + OH → CH3CH2OH + COCH3 (B) CH2CH2SCHz + OH → CH3CH2OH + SCH; (C) CH3CH2N(CH3)2 + OH -- CH3CH2OH + "N(CH3)2 (D) O CH3CH2OSC6H.CH3 + OH - © CHỊCH,OH + OSCH,CH
I got A, C, D, & E incorrect i put A: 3-methylenehexane C:(3E,5E)-2,6-dimethylocta-1,3,5-triene D:(E)-4-ethylhept-3-ene E: 1-cyclohexylcyclohexa-1,3-diene...
I got A, C, D, & E incorrect
i put
A: 3-methylenehexane
C:(3E,5E)-2,6-dimethylocta-1,3,5-triene
D:(E)-4-ethylhept-3-ene
E: 1-cyclohexylcyclohexa-1,3-diene
i need the correct names, my input answers were
incorrect.
CHAPTER 7 Structure and Synthesis of Alkenes -32 Give a correct name for each compound. () (CH2CH2)2C=CHCH; (c) (a) CH-CH2-C-CH-CH2-CH CH CHCI
4. assign common and IUPAC names for the following ethers 5. answer the following questions using...
4. assign common and IUPAC names for the following
ethers
5. answer the following questions using complete
sentences
6. assign IUPAC names to the following aldehydes and
keytones
*ketones
CH,CH,CH- 0- CHCH,CH, 5. Answer the following questions using complete sentences: a. Why does hydrogen bonding not take place between molecule of aldehydes or ketones b. The boiling point of propanal is 49°C, whereas the boiling point of propanol is 97 °C. Explain this difference in boiling points. 6. Assign IUPAC...
option D is correct, please explain why it is not any of the other options. 5....
option D is correct, please explain why it is not any of the other
options.
5. Which of the following statements applies to the E2 mechanism? a) It occurs with inversion of stereochemistry. b) It occurs with racemization of stereochemistry. c) It proceeds through the more stable carbocation intermediate. d) The C-H and C-X bonds that break must be anti. e) Use of a bulky base gives the more highly substituted alkene product.
Please explain clearly why the answer is correct Which of these "curved arrows" describe a mechanism...
Please explain clearly why the answer is correct
Which of these "curved arrows" describe a mechanism for the formation of a carbocation that has roughly the same stability as this one? HHH - H- C- C 70-I CH H H-C-H Н AA only [B] B only [C] C only [D] B and C only [E] A and C only Explanation for your choice (4 pts)
Organic Chemistry please help asap 70. What nucleophiles wou cleophiles would form the following compounds as...
Organic Chemistry please help asap
70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...
When trans-1,2-Dibromocyclopentane is treated with NaNH/NH A, 1-Bromocyclopentene is formed. What product would be expected and...
When trans-1,2-Dibromocyclopentane is treated with NaNH/NH A, 1-Bromocyclopentene is formed. What product would be expected and why does 1-Bromocyclopentene form instead? 58. Briefly but completely describe where and what should be "seen" in the following spectra for I-Ethoxy-4. bromobenzene Mass Spec IR H NMR "C NMR 42. Which of the following is the most stable carbocation? CH3 CH CH CH CH HCHHCHCHCH CCHCH-CH CH CH2-CHCH-CH CH CH3 CH, A. D. B. 43. Which of the following is an example of...
1) What is the product of the following aldol addition of two aldehydes reaction Өон CH.CH.CH сн,сн: снҫнн CH. B) CH:CH.CHCHH сн: Сн, он cң, сн: сненнн СН: D) cң, сн: Снінен CH₃CH: E) он cң, cң сн: Снінен сн: 2) Draw the enone product of the following reaction: HO, HO, 3 HC CH HỌC CH 3) What is the product of the following crossed aldol addition reaction? "ОН CH, CHỊCH + H C H (excess) CH3CH2CHCH IV. CH3CHCH Сн,он...
the weakest base: CH3 HO HS the fastest in an Syl reaction: (CE)_CACHOSCH (CH3CB (CH.) CHCH(Br)CH, (CH),C(Br)CH (CH3)2CHCH Br 2. For each pair of reactions given below indicate which is faster and explain your reasoning. + CHỊ N + C CH3Cl + N CH3 + Ng CH₃N₂ + i CHg. + NaCN CH, CN + Nal DMSO CH3-1 + NaCN C H, CN + Nal Cho (c) CH,0 + CH,CH,Br - HƠ + CHỊCH,Br CH,CH,OCH, + Bril CH,CH,OH + Br...
Please explain how you got the answer
What are the products implied by the two different mechanistic pathways shown here? PATHWAYA CHCH, - PATHWAY B A + B HECH CHCH CH снен TIT [B] A is II: B is! [E] A is III: B is IV [C] A is l; B is III [A] A is II: B is III [D] A is 1. Bis IV Explanation for your choice (4 pts) Which of these "curved arrows" describe a mechanism...
organic chemistry
answer is D.
Can someone please explain why?
3. Which reaction would proceed the fastest? (A) CH3CH2OCH2 + OH → CH3CH2OH + COCH3 (B) CH2CH2SCHz + OH → CH3CH2OH + SCH; (C) CH3CH2N(CH3)2 + OH -- CH3CH2OH + "N(CH3)2 (D) O CH3CH2OSC6H.CH3 + OH - © CHỊCH,OH + OSCH,CH
I got A, C, D, & E incorrect
i put
A: 3-methylenehexane
C:(3E,5E)-2,6-dimethylocta-1,3,5-triene
D:(E)-4-ethylhept-3-ene
E: 1-cyclohexylcyclohexa-1,3-diene
i need the correct names, my input answers were
incorrect.
CHAPTER 7 Structure and Synthesis of Alkenes -32 Give a correct name for each compound. () (CH2CH2)2C=CHCH; (c) (a) CH-CH2-C-CH-CH2-CH CH CHCI
4. assign common and IUPAC names for the following
ethers
5. answer the following questions using complete
sentences
6. assign IUPAC names to the following aldehydes and
keytones
*ketones
CH,CH,CH- 0- CHCH,CH, 5. Answer the following questions using complete sentences: a. Why does hydrogen bonding not take place between molecule of aldehydes or ketones b. The boiling point of propanal is 49°C, whereas the boiling point of propanol is 97 °C. Explain this difference in boiling points. 6. Assign IUPAC...
option D is correct, please explain why it is not any of the other
options.
5. Which of the following statements applies to the E2 mechanism? a) It occurs with inversion of stereochemistry. b) It occurs with racemization of stereochemistry. c) It proceeds through the more stable carbocation intermediate. d) The C-H and C-X bonds that break must be anti. e) Use of a bulky base gives the more highly substituted alkene product.
Please explain clearly why the answer is correct
Which of these "curved arrows" describe a mechanism for the formation of a carbocation that has roughly the same stability as this one? HHH - H- C- C 70-I CH H H-C-H Н AA only [B] B only [C] C only [D] B and C only [E] A and C only Explanation for your choice (4 pts)
Organic Chemistry please help asap
70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...
When trans-1,2-Dibromocyclopentane is treated with NaNH/NH A, 1-Bromocyclopentene is formed. What product would be expected and why does 1-Bromocyclopentene form instead? 58. Briefly but completely describe where and what should be "seen" in the following spectra for I-Ethoxy-4. bromobenzene Mass Spec IR H NMR "C NMR 42. Which of the following is the most stable carbocation? CH3 CH CH CH CH HCHHCHCHCH CCHCH-CH CH CH2-CHCH-CH CH CH3 CH, A. D. B. 43. Which of the following is an example of...
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