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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?...
the answers i circled are incorrect. can you give me the
correct answers and explain why?
postural de Pero ss and so Lalash, an walach asymmetric carbon as Ror S. (3) label the How many asymmetric carbon atoms are present in the following compound A) B) 1 D) 3 E) 4 2) Which of the statements below correctly describes an achiral molecule? The molecule has a nonsuperimposable mirror image. B) The molecule exhibits optical activity when it interacts with plane-polarized...
the answers i circled are incorrect. can you give me all the correct answers and explain...
the answers i circled are incorrect. can you give me all the
correct answers and explain why?
2) Which of the statements below correctly describes an achiral molecule? A The molecule has a nonsuperimposable mirror image. cule exhibits optical activity when it interacts with plane-polarized light. C) The molecule has an enantiomer. D) The molecule might be a meso form. E) None of the above 3) Predict the specific rotation of the compound shown. CH нс 4 A) It is...
the answers i circled are incorrect except for 19. can you please tell me why this...
the answers i circled are incorrect except for 19. can you
please tell me why this is correct. can you give me the correct
answers and explain why?
actions usually proceed with amounts of inversion and retention at the center undergoing sustitution more inversion than retention at the center undergoing substitution y more retention then in version at the center undergoing substitution lete inversion at the center undergoing sostituti plete retention at the center undergoing substitution Which of the following...
Please provide answers to the questions that are circled. Thank you! Least reactive Most reactive 12.53)...
Please provide answers to the questions that are circled.
Thank you!
Least reactive Most reactive 12.53) A standard method for preparing sodium cyclopentadienide (C H Na) is by the reaction of cyclopentadiene with a solution of NaNH, in liquid ammonia. Write a net ionic equation for this reaction, identify the acid and the base, and use curved arrows to track the flow of electrons. 12.54 The same anion is formed by loss of the most acidic proton from 1-methyl-1,3- cyclopentadiene...
the answers i circled are incorrect except for 13. i know 11 is d and 15 is a. can you please explain why these three a...
the answers i circled are incorrect except for 13. i know 11
is d and 15 is a. can you please explain why these three are
correct as well. can you give me the correct answers and explain
why?
de motor and h ow w generation recognized disorder that can benefit from hippothy wy b o cice to which they were anached indiactive donation of electron density to the cationic center chan inductive removal of electron density from the w...
can someone explain these? I have difficulties eith mechanisms. thank you 10. For each of the...
can
someone explain these? I have difficulties eith mechanisms. thank
you
10. For each of the following reactions, draw the structure of the major organic product in the box provided. Each numbered set of reagents above or below the arrow represents a complete separate reaction. For multi-step reactions, give only the structure of the final product a) KOCH,CH HOCH.CH b) кови KOtBu HOtBu OTS EtOAc ОТf - сн, -Br сн, снен, KOCH.CH HOCH.CH н DMF кон (alc) DMSO KOtBu Нова...
can you give me the correct answers with explanations? 7. Snl reactions usually proceed with athons...
can you give me the correct answers with
explanations?
7. Snl reactions usually proceed with athons a rectn equal amounts of inversion and retention at the center undergoing substitution. slightly more inversion than retention at the center undergoing substitution. ntly more retention then inversion at the center undergoing substitution. (D) (E) sligh complete inversion at the center undergoing substitution. complete retention at the center undergoing substitution How many distinct alkene products are possible when the alkyl bromide below undergoes E2...
the answers i circled are incorrect except for number 10. i know number 8 is d....
the answers i circled are incorrect except for number 10. i
know number 8 is d. for those two can you explain why the answer is
that? can you give me the correct answers and explain why?
ren with Down Syndrome waren with local deve we described as generat ) lam towan l and e ch rochemical court of Th correct configuration? is RS). Which offi ces corresponds OH OM HOCH,HOH I WHER TNH, CH, HO CH, w AT 111...
Can you please explain why D is correct and other answers are incorrect? Thank you Which...
Can you please explain why D is correct and other answers are
incorrect? Thank you
Which alcohol will undergo acid-catalyzed dehydration under the mildest conditions? 56. (A) CH CH,CH,CH,OH (B) CH,CH2CH OH)CH3 (C) (CH)CHCHOH ( (CH),COH
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
the answers i circled are incorrect. can you give me the
correct answers and explain why?
postural de Pero ss and so Lalash, an walach asymmetric carbon as Ror S. (3) label the How many asymmetric carbon atoms are present in the following compound A) B) 1 D) 3 E) 4 2) Which of the statements below correctly describes an achiral molecule? The molecule has a nonsuperimposable mirror image. B) The molecule exhibits optical activity when it interacts with plane-polarized...
the answers i circled are incorrect. can you give me all the
correct answers and explain why?
2) Which of the statements below correctly describes an achiral molecule? A The molecule has a nonsuperimposable mirror image. cule exhibits optical activity when it interacts with plane-polarized light. C) The molecule has an enantiomer. D) The molecule might be a meso form. E) None of the above 3) Predict the specific rotation of the compound shown. CH нс 4 A) It is...
the answers i circled are incorrect except for 19. can you
please tell me why this is correct. can you give me the correct
answers and explain why?
actions usually proceed with amounts of inversion and retention at the center undergoing sustitution more inversion than retention at the center undergoing substitution y more retention then in version at the center undergoing substitution lete inversion at the center undergoing sostituti plete retention at the center undergoing substitution Which of the following...
Please provide answers to the questions that are circled.
Thank you!
Least reactive Most reactive 12.53) A standard method for preparing sodium cyclopentadienide (C H Na) is by the reaction of cyclopentadiene with a solution of NaNH, in liquid ammonia. Write a net ionic equation for this reaction, identify the acid and the base, and use curved arrows to track the flow of electrons. 12.54 The same anion is formed by loss of the most acidic proton from 1-methyl-1,3- cyclopentadiene...
the answers i circled are incorrect except for 13. i know 11
is d and 15 is a. can you please explain why these three are
correct as well. can you give me the correct answers and explain
why?
de motor and h ow w generation recognized disorder that can benefit from hippothy wy b o cice to which they were anached indiactive donation of electron density to the cationic center chan inductive removal of electron density from the w...
can
someone explain these? I have difficulties eith mechanisms. thank
you
10. For each of the following reactions, draw the structure of the major organic product in the box provided. Each numbered set of reagents above or below the arrow represents a complete separate reaction. For multi-step reactions, give only the structure of the final product a) KOCH,CH HOCH.CH b) кови KOtBu HOtBu OTS EtOAc ОТf - сн, -Br сн, снен, KOCH.CH HOCH.CH н DMF кон (alc) DMSO KOtBu Нова...
can you give me the correct answers with
explanations?
7. Snl reactions usually proceed with athons a rectn equal amounts of inversion and retention at the center undergoing substitution. slightly more inversion than retention at the center undergoing substitution. ntly more retention then inversion at the center undergoing substitution. (D) (E) sligh complete inversion at the center undergoing substitution. complete retention at the center undergoing substitution How many distinct alkene products are possible when the alkyl bromide below undergoes E2...
the answers i circled are incorrect except for number 10. i
know number 8 is d. for those two can you explain why the answer is
that? can you give me the correct answers and explain why?
ren with Down Syndrome waren with local deve we described as generat ) lam towan l and e ch rochemical court of Th correct configuration? is RS). Which offi ces corresponds OH OM HOCH,HOH I WHER TNH, CH, HO CH, w AT 111...
Can you please explain why D is correct and other answers are
incorrect? Thank you
Which alcohol will undergo acid-catalyzed dehydration under the mildest conditions? 56. (A) CH CH,CH,CH,OH (B) CH,CH2CH OH)CH3 (C) (CH)CHCHOH ( (CH),COH
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
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