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 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
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...
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
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...
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...
Could anyone please explain why letter A has E2 included? I thought it was soley Sn2...
Could anyone please explain why letter A has E2 included? I
thought it was soley Sn2 (or at least the majority of it).
Thanks!
Draw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry, if the product is racemic indicate this by either drawing both enantiomers or drawing one and writing racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'.
identify which compound is more acidic and explain your choice. or each of the following compounds,...
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
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 explain why
122 Nuclear Magnetic Resonance Spectroscopy - Part One: Baci which compound is a stronger Bronsted-lowry base. Explain why? puridine purrole
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...
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
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...
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...
Could anyone please explain why letter A has E2 included? I
thought it was soley Sn2 (or at least the majority of it).
Thanks!
Draw the structure of the expected organic product(s) formed in the following reactions including correct stereochemistry, if the product is racemic indicate this by either drawing both enantiomers or drawing one and writing racemic. Assume all reagents listed are present in excess unless otherwise noted. If no reaction occurs, state 'No Reaction'.
identify which compound is more acidic and explain your choice. or each of the following compounds, Make sure you include structures of these which compounds in your answers ounds, 1. F (e) 24-Dimethy-3,5-hepanedione or 4, 4-Dimethy)-3,5-heptanedione (b) 1.2-Cyclopentanedione or 1,3-cyclopentanedione 2. When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (z) positions. identily which gamma position is deprotonated, and explain why the y proton is the most acidie proton in the compound. 3. Rank...
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