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(a) The two molecules below are structurally similar, however, one of these molecules is much more...
Organic Chemistry 4. Below are two molecules, B and C. Explain the differences in pKa of...
Organic Chemistry
4. Below are two molecules, B and C. Explain the differences in pKa of the two molecules by drawing the conjugate base of molecule C and a resonance structure that would not be found in molecule B. Hint: Draw out the NO2 group. conjugate base of molecule C pKa- 29.5 molecule B NO2 pka= 8.6 molecule C 5. Below is the molecule Abilify, which is a top selling drug that is used to treat schizophrenia, bipolar disorder and...
7. One of the following is much more acidic than the other. Circle the more acidic...
7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) Acidity of one pf the it's shown 8. For the reaction show, a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures for the intermediate (4 pts) Br...
Acetonitrile (CH3CN) has a pK, of 25, making it more acidic than many other compounds having...
Acetonitrile (CH3CN) has a pK, of 25, making it more acidic than many other compounds having only C-H bonds. Draw structures for acetonitrile and its conjugate base using skeletal structures. Use resonance structures to account for the acidity of acetonitrile. draw structure ... Acetonitrile Acetonitrile's conjugate base: draw structure... draw structure ... (negative charge on ) (negative charge on N) The acidity of acetonitrile is accounted for by: O Acetonitrile's conjugate base is stabilized by resonance. O Acetonitrile's conjugate base...
7-9 please! 4 7. One of the following is much more acidic than the other. Circle...
7-9 please!
4 7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) H Acidity of one pf the H's shown H H 8. For the reaction show a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control" product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures...
Explain why cyclopentadiene (pKa 16) is many orders of magnitude more acidic than cyclopentane (pKa >...
Explain why cyclopentadiene (pKa 16) is many orders of
magnitude more acidic than cyclopentane (pKa > 50). (Hint: Draw
the structural formula for the anion formed by removing one of the
protons on the −CH2− group, and then apply the Hückel criteria for
aromaticity.)
Explain why cyclopentadiene (PK, 16) is many orders of magnitude more acidic than cyclopentane (pka > 50). (Hint: Draw the structural formula for the anion formed by removing one of the protons on the -CH2- group,...
Can you please explain these throughly!! I will give good rate thank you!! For the next...
Can you please explain these throughly!! I will give good rate
thank you!!
For the next problems, your explanation needs to refer to one or more of the following factors: inductive, electronegativity, resonance stability, size 3. The following compounds can all behave as acids: 0 0 OH CH3CH2OH F C HCOH HOCF3 HC 0 a. For each compound, draw its conjugate base. b. Rank the acids in order of increasing acidity. Explain your ranking, 4. The following compounds can all...
For the next problems, your explanation needs to refer to one or more of the following...
For the next problems, your explanation needs to refer to one or more of the following factors: inductive, electronegativity, resonance stability, size 3. The following compounds can all behave as acids: O HC OH HOCF3unhoOH CH3CH2OH E a. For each compound, draw its conjugate base. b. Rank the acids in order of increasing acidity. Explain your ranking.
Add curved arrows to show how the compound on the left is converted to the compound...
Add curved arrows to show how the compound on the left is
converted to the compound on the right.
Squaric acid has a pKa of 1.5, making it much more acidic than many carboxylic acids (typical pKa values of 4-5). One of the reasons for its acidity is resonance stabilization of its conjugate base. which is shown below. Add curved arrows to the structure on the left to show how it is converted to the other resonance contributor shown to...
lel For the next problems, your explanation needs to refer to one or more of the...
lel For the next problems, your explanation needs to refer to one or more of the following factors: inductive, electronegativity, resonance stability, size 3 The following compounds can all behave as acids O FaC OH CHCH2OH CF H3C Он но н.с Он For each compound, draw its conjugate base. a. Explain your ranking Rank the acids in order of increasing acidity. b. 4. The following compounds can all behave as hases: NaOH CH CH2OH NANH2 CH CH2NH NH2 For each...
need help 4. Assume that you have samples of the following two molecules, both with the...
need help
4. Assume that you have samples of the following two molecules, both with the formula CsH160. a) Suppose you are given one of the above molecules (but not both). How could you use an oxidation reaction to determine which molecule you have? Briefly explain with text and reasonable sketches. b) Suppose you are given one of the above molecules (but not both). How could you use dehydration reaction to determine which molecule you have? Briefly explain with text...
Organic Chemistry
4. Below are two molecules, B and C. Explain the differences in pKa of the two molecules by drawing the conjugate base of molecule C and a resonance structure that would not be found in molecule B. Hint: Draw out the NO2 group. conjugate base of molecule C pKa- 29.5 molecule B NO2 pka= 8.6 molecule C 5. Below is the molecule Abilify, which is a top selling drug that is used to treat schizophrenia, bipolar disorder and...
7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) Acidity of one pf the it's shown 8. For the reaction show, a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures for the intermediate (4 pts) Br...
Acetonitrile (CH3CN) has a pK, of 25, making it more acidic than many other compounds having only C-H bonds. Draw structures for acetonitrile and its conjugate base using skeletal structures. Use resonance structures to account for the acidity of acetonitrile. draw structure ... Acetonitrile Acetonitrile's conjugate base: draw structure... draw structure ... (negative charge on ) (negative charge on N) The acidity of acetonitrile is accounted for by: O Acetonitrile's conjugate base is stabilized by resonance. O Acetonitrile's conjugate base...
7-9 please!
4 7. One of the following is much more acidic than the other. Circle the more acidic one, and explain very briefly why? (3 points) H Acidity of one pf the H's shown H H 8. For the reaction show a. Write "1,2" underneath and "1,4" underneath the appropriate products. (1 pt) b. Write "thermodynamic" underneath the appropriate "thermodynamic control" product (1 pt) c. Draw the mechanism for the reaction, using formal arrow pushing. Draw both resonance structures...
Explain why cyclopentadiene (pKa 16) is many orders of
magnitude more acidic than cyclopentane (pKa > 50). (Hint: Draw
the structural formula for the anion formed by removing one of the
protons on the −CH2− group, and then apply the Hückel criteria for
aromaticity.)
Explain why cyclopentadiene (PK, 16) is many orders of magnitude more acidic than cyclopentane (pka > 50). (Hint: Draw the structural formula for the anion formed by removing one of the protons on the -CH2- group,...
Can you please explain these throughly!! I will give good rate
thank you!!
For the next problems, your explanation needs to refer to one or more of the following factors: inductive, electronegativity, resonance stability, size 3. The following compounds can all behave as acids: 0 0 OH CH3CH2OH F C HCOH HOCF3 HC 0 a. For each compound, draw its conjugate base. b. Rank the acids in order of increasing acidity. Explain your ranking, 4. The following compounds can all...
For the next problems, your explanation needs to refer to one or more of the following factors: inductive, electronegativity, resonance stability, size 3. The following compounds can all behave as acids: O HC OH HOCF3unhoOH CH3CH2OH E a. For each compound, draw its conjugate base. b. Rank the acids in order of increasing acidity. Explain your ranking.
Add curved arrows to show how the compound on the left is
converted to the compound on the right.
Squaric acid has a pKa of 1.5, making it much more acidic than many carboxylic acids (typical pKa values of 4-5). One of the reasons for its acidity is resonance stabilization of its conjugate base. which is shown below. Add curved arrows to the structure on the left to show how it is converted to the other resonance contributor shown to...
lel For the next problems, your explanation needs to refer to one or more of the following factors: inductive, electronegativity, resonance stability, size 3 The following compounds can all behave as acids O FaC OH CHCH2OH CF H3C Он но н.с Он For each compound, draw its conjugate base. a. Explain your ranking Rank the acids in order of increasing acidity. b. 4. The following compounds can all behave as hases: NaOH CH CH2OH NANH2 CH CH2NH NH2 For each...
need help
4. Assume that you have samples of the following two molecules, both with the formula CsH160. a) Suppose you are given one of the above molecules (but not both). How could you use an oxidation reaction to determine which molecule you have? Briefly explain with text and reasonable sketches. b) Suppose you are given one of the above molecules (but not both). How could you use dehydration reaction to determine which molecule you have? Briefly explain with text...
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