Could anyone explain why the first compound is more stable than the one I circled? And also, why is resonance a stronger influence and not induction? Thanks!
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Could anyone explain why the first compound is more stable than
the one I circled? And...
Can someone please explain this! 15. Circle one of the following charged compounds which is most stable. (3 Points) Sle...
Can someone please explain this!
15. Circle one of the following charged compounds which is most stable. (3 Points) Sleast acidic +2 Which is the stronger influence for your choice? a) Resonance or b) Induction hyperconjugation)? (2 Points)
Explain why compound A is more acidic using resonance structures and question 21. WILLUDUlyalli Clemsty ENAM...
Explain why compound A is more acidic using resonance structures
and question 21.
WILLUDUlyalli Clemsty ENAM 20. Explain why Compound A is more acidic than Compound B. Use resonance structures to e 21. Which of the following is the least stable carbocation? Circle your response. (2) IV
1. What is a structure based explanation for why acetamide is more stable than acetone. I'm...
1. What is a structure based explanation for why acetamide is
more stable than acetone. I'm pretty sure it has to do with
resonance.
2. also for question F im fairly sure it has to do with
resonance again but I not sure exactly why. could someone answer
and explain?
F. Draw the conjugate base for each compound below and draw the appropriate structures to explain the difference in N-H acidity pKa~9.5 pKa 16 N-H N-H
Please help! 4. Suppose Compound B is the conjugate base of Compound A. Calculate the approximate...
Please help!
4. Suppose Compound B is the conjugate base of Compound A. Calculate the approximate concentration of Compound A that must be present in a 0.042 M solution of Compound B to produce a pH of 4.96. The K. for Compound A is 1.8 x 109. Show your work. Round your final answer to the nearest hundredth decimal place. (5pts) 5. Consider the structure below. Then using the empty boxes, answer parts (a)-(e). HO (a) (1 pts) Draw a...
please explain why 122 Nuclear Magnetic Resonance Spectroscopy - Part One: Baci which compound is a stronger Bronste...
please explain why
122 Nuclear Magnetic Resonance Spectroscopy - Part One: Baci which compound is a stronger Bronsted-lowry base. Explain why? puridine purrole
Explain this resonance and basicity problem? Why does the Guanidine top nitrogen have a negative dipole?...
Explain this resonance and basicity problem? Why does the
Guanidine top nitrogen have a negative dipole? Doesn't the
resonance hybrid cause the bond to be less than 1 full bond so it
causes it to be a positive dipole? Also doesn't the resonance in
guanidine cause it to be a weaker base than ammonia?
17. (5) Let's decide which is the stronger base ammonia or guanidine. Circle one answer each in H2N parts (a) (c) below. Guanidine (a) What is...
Which of the choices explains why one nucleophile is stronger than another nucleophile? More than one...
Which of the choices explains why one nucleophile is stronger than another nucleophile? More than one answer is possible. It is also possible that NONE of these is correct. 7 A stronger nucleophile is larger than another nucleophile. A stronger nucleophile has a less electronegative nucleophilic atom than another nucleophile. A stronger nucleophile has less steric hindrance than another nucleophile. Using this information, in methanol, CH3OH, which of the following is a stronger nucleophile, trimethylamine, (CH3)3N, or dimethylether, (CH3)20? SS...
2.2 Nitromethane (CH3NO2, pka = 10) is more acidic than most organic acids. Explain why nitromethane...
2.2 Nitromethane (CH3NO2, pka = 10) is more acidic than most organic acids. Explain why nitromethane is so much more acidic than ethane (pka = 60). Write the chemical equations to illustrate the acidity of the compounds. Include valid Lewis dot structures (including formal charge) and resonance structures, if relevant. (6)
Can anyone explain why it's FeCrO4 instead of Fe2(CrO4)2? please explain more details as possible, i...
Can anyone explain why it's FeCrO4 instead of
Fe2(CrO4)2?
please explain more details as possible, i will give
upvote.
Write the empirical formula for at least four ionic compounds that could be formed from the following ions: Fe2+, Fe3+, CroC,H,02 C,H02 Croz Fe3+Fe(C2H,02), Fez (C+04) Fe2+Fe(C2H,02), FeCrO 4
Could you explain why too? Thank you. Which of the compounds is more soluble in an acidic solution than in pure water? C...
Could you explain why too? Thank you.
Which of the compounds is more soluble in an acidic solution than in pure water? CuBr Zn(OH)2 Srs CuCN RbC104
Can someone please explain this!
15. Circle one of the following charged compounds which is most stable. (3 Points) Sleast acidic +2 Which is the stronger influence for your choice? a) Resonance or b) Induction hyperconjugation)? (2 Points)
Explain why compound A is more acidic using resonance structures
and question 21.
WILLUDUlyalli Clemsty ENAM 20. Explain why Compound A is more acidic than Compound B. Use resonance structures to e 21. Which of the following is the least stable carbocation? Circle your response. (2) IV
1. What is a structure based explanation for why acetamide is
more stable than acetone. I'm pretty sure it has to do with
resonance.
2. also for question F im fairly sure it has to do with
resonance again but I not sure exactly why. could someone answer
and explain?
F. Draw the conjugate base for each compound below and draw the appropriate structures to explain the difference in N-H acidity pKa~9.5 pKa 16 N-H N-H
Please help!
4. Suppose Compound B is the conjugate base of Compound A. Calculate the approximate concentration of Compound A that must be present in a 0.042 M solution of Compound B to produce a pH of 4.96. The K. for Compound A is 1.8 x 109. Show your work. Round your final answer to the nearest hundredth decimal place. (5pts) 5. Consider the structure below. Then using the empty boxes, answer parts (a)-(e). HO (a) (1 pts) Draw a...
please explain why
122 Nuclear Magnetic Resonance Spectroscopy - Part One: Baci which compound is a stronger Bronsted-lowry base. Explain why? puridine purrole
Explain this resonance and basicity problem? Why does the
Guanidine top nitrogen have a negative dipole? Doesn't the
resonance hybrid cause the bond to be less than 1 full bond so it
causes it to be a positive dipole? Also doesn't the resonance in
guanidine cause it to be a weaker base than ammonia?
17. (5) Let's decide which is the stronger base ammonia or guanidine. Circle one answer each in H2N parts (a) (c) below. Guanidine (a) What is...
Which of the choices explains why one nucleophile is stronger than another nucleophile? More than one answer is possible. It is also possible that NONE of these is correct. 7 A stronger nucleophile is larger than another nucleophile. A stronger nucleophile has a less electronegative nucleophilic atom than another nucleophile. A stronger nucleophile has less steric hindrance than another nucleophile. Using this information, in methanol, CH3OH, which of the following is a stronger nucleophile, trimethylamine, (CH3)3N, or dimethylether, (CH3)20? SS...
2.2 Nitromethane (CH3NO2, pka = 10) is more acidic than most organic acids. Explain why nitromethane is so much more acidic than ethane (pka = 60). Write the chemical equations to illustrate the acidity of the compounds. Include valid Lewis dot structures (including formal charge) and resonance structures, if relevant. (6)
Can anyone explain why it's FeCrO4 instead of
Fe2(CrO4)2?
please explain more details as possible, i will give
upvote.
Write the empirical formula for at least four ionic compounds that could be formed from the following ions: Fe2+, Fe3+, CroC,H,02 C,H02 Croz Fe3+Fe(C2H,02), Fez (C+04) Fe2+Fe(C2H,02), FeCrO 4
Could you explain why too? Thank you.
Which of the compounds is more soluble in an acidic solution than in pure water? CuBr Zn(OH)2 Srs CuCN RbC104
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