Homework Answers
a) KOH can depronate phenol since hydroxyl ion is a stronger base
b)phenol react with ammonia since ammonia is sufficient basic ( due to presence of loan pair over nitrogen) to deprotonate phenol.
c) phenol does not react with NaHCO3 since bicarbonate ion is a weak base and can't remove proton from phenol.
d) NaH can deprotonate phenol since hydride ion is a strong base.
so correct answer is ( a,b,d )
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please explain your answers 6. Circle all of the bases below that can be used successfully to deprotonate phenol (C...
please explain your answers 5. Circle all of the bases below that can be used successfully...
please explain your answers
5. Circle all of the bases below that can be used successfully to deprotonate CH3OH. (0.3 pts) a. CH3CO2Na b. KOH C. NH3 d. NaHCO3 e. NaNH2 f. NaH
please explain your answers 3. Circle the stronger base in each pair. (0.2 pts ea = 2.0 pts) a. (CH3) 3COK vs. CH3O...
please explain your answers
3. Circle the stronger base in each pair. (0.2 pts ea = 2.0 pts) a. (CH3) 3COK vs. CH3OK b. HCECNa vs. CH3CH2ONa c. NaNH2 vs. HCECNA d. NaCN vs. NaI e. NAHCO3 vs. NaOH f. NaOH vs. C6H5CO2Na g. C6H5CO2Na vs. C6H5ONa h. CH3CO2Na vs. CH3ONa i. CH3ONa vs. NaH j. NH3 vs. CH3CO2Na
please explain your answers 3. Circle the stronger base in each pair. (0.2 pts ea = 2,0 pts) a. (CH3) COK vs. CH3OK...
please explain your answers
3. Circle the stronger base in each pair. (0.2 pts ea = 2,0 pts) a. (CH3) COK vs. CH3OK b. HCECNa vs. CH3CH2ONa c. NaNH2 vs. HCECNa d. NacN vs. NaI e. NaHCO3 vs. NaOH f. NaOH vs. CoH5CO2Na g. C.H.COŻNa vs. CoHsONa h. CH3CO2Na vs. CHEONa u dotos i. CH3ONa vs. Nah j. NH3 vs. CH3CO2Na
Circle the stronger base in each pair- answers only. No explanations, no incomplete answers. 3. Circle...
Circle the stronger base in each pair- answers only. No
explanations, no incomplete answers.
3. Circle the stronger base in each pair. (0.2 pts ea 2.0 pts) a. (CH3) 3COK vs. CH3OK b. HCECNa vs. CH3CH2ONa c. NaNH2 vs. HCECNa d. NaCN vs. NaI e. NaHCO3 vs. NaOH CoH5CO2Na f. NaOH VS. g. C6H5CO2Na vs. CoH5ONa h. CH3CO2NA vs. CH3ONa CH3ONA vs. NaH i. NH3 vs. CH3CO2Na j.
Provide answers to ALL of the questions below please: (a) Compare the acidity of phenol with...
Provide answers to ALL of the questions below please:
(a) Compare the acidity of phenol with that of p-nitrophenol. Explain and illustrate your answer with diagrams. OH OH NO2 5 marksl (b) Use molecular orbital (MO) theory diagrams to illustrate the aromaticity of benzene and the lack of aromaticity of cyclooctatetraene. 15 marksl (c) Explain the difference between 1,2-addition and 1.4-(ie, conjugate addition) to α,β- unsaturated carbonyl compounds, using mechanisms to illustrate your answer. 5 marks
Please explain how to find the answers Write the formulas of the conjugate bases of the...
Please explain how to find the answers
Write the formulas of the conjugate bases of the acids below and name everything H2SO4 HNO3 HCI CH3COOH NHA HOCI Write the formulas of the conjugate acids of the bases below and name everything NH3 OH co,2 CH3COO HSO OCI For each of the neutral salts below, indicate whether their aqueous solutions are acid, basic, or neutral NH4CI KF Na2CO3 . In a 0.15 M solution of NaOH in water at 25 °C,...
please explain your answer 4. This question continues on the next page. For each of the...
please explain your answer
4. This question continues on the next page. For each of the following acid-base reactions: (0.3 pts ea = 3.0 pts) a. Predict the products that could form. b. Next to the products you draw, write either "Products not favored" or "Products favored." a. CH3OH + NaH → b. NaOH + CH3OH → C. KOH + (CH3)3COH → d. CH3OH + HI → dan gelen o e. HCECNa + CH3CH2OH → TH f. HCECH + CH3Li...
Circle the stronger BASE in each pair. No explanation, no incomplete answers. I have 4 of these correct so I will know...
Circle the stronger BASE in each pair. No explanation, no
incomplete answers. I have 4 of these correct so I will know if
you’re getting them wrong.
3. Circle the stronger base in each pair. (0.2 pts ea = 2.0 pts) a. (CH3) 3COK vs. CH3OK b. HCECNa vs. CH3CH2ONa C. NaNH2 vs. HCECNa d. NacN vs. NaI e. NaHCO3 vs. NaOH f. NaOH vs. CoH5CO2Na g. C6H5COzNa vs. CoH5ONa h. CH3CO2Na vs. CH3ONa i. CH3ONa vs. NaH j. NH3...
please explain! Problem 1 (30 pts) a) Name the compound shown below: CH3 CI b) Circle...
please explain!
Problem 1 (30 pts) a) Name the compound shown below: CH3 CI b) Circle the alcohol that would dehydrate the fastest in H2SO4. به ما مبل c) Circle the products of the reaction below. پر20 1) KMnO4. KOH heat 2) HO* OH ) * ريم d) Circle the correct order of stability for the alkenes? V VV V V >c>b
I have the answers but can you explain please ? Circle the stereoisomer that is the...
I have the answers but can you explain please ?
Circle the stereoisomer that is the more stable compound? Explain your answer by drawing the most stable chair conformer of each compound using the partial chair structures below. Your equitorial and axial substituents must be unambiguous (if they're not, please label them).
please explain your answers
5. Circle all of the bases below that can be used successfully to deprotonate CH3OH. (0.3 pts) a. CH3CO2Na b. KOH C. NH3 d. NaHCO3 e. NaNH2 f. NaH
please explain your answers
3. Circle the stronger base in each pair. (0.2 pts ea = 2.0 pts) a. (CH3) 3COK vs. CH3OK b. HCECNa vs. CH3CH2ONa c. NaNH2 vs. HCECNA d. NaCN vs. NaI e. NAHCO3 vs. NaOH f. NaOH vs. C6H5CO2Na g. C6H5CO2Na vs. C6H5ONa h. CH3CO2Na vs. CH3ONa i. CH3ONa vs. NaH j. NH3 vs. CH3CO2Na
please explain your answers
3. Circle the stronger base in each pair. (0.2 pts ea = 2,0 pts) a. (CH3) COK vs. CH3OK b. HCECNa vs. CH3CH2ONa c. NaNH2 vs. HCECNa d. NacN vs. NaI e. NaHCO3 vs. NaOH f. NaOH vs. CoH5CO2Na g. C.H.COŻNa vs. CoHsONa h. CH3CO2Na vs. CHEONa u dotos i. CH3ONa vs. Nah j. NH3 vs. CH3CO2Na
Circle the stronger base in each pair- answers only. No
explanations, no incomplete answers.
3. Circle the stronger base in each pair. (0.2 pts ea 2.0 pts) a. (CH3) 3COK vs. CH3OK b. HCECNa vs. CH3CH2ONa c. NaNH2 vs. HCECNa d. NaCN vs. NaI e. NaHCO3 vs. NaOH CoH5CO2Na f. NaOH VS. g. C6H5CO2Na vs. CoH5ONa h. CH3CO2NA vs. CH3ONa CH3ONA vs. NaH i. NH3 vs. CH3CO2Na j.
Provide answers to ALL of the questions below please:
(a) Compare the acidity of phenol with that of p-nitrophenol. Explain and illustrate your answer with diagrams. OH OH NO2 5 marksl (b) Use molecular orbital (MO) theory diagrams to illustrate the aromaticity of benzene and the lack of aromaticity of cyclooctatetraene. 15 marksl (c) Explain the difference between 1,2-addition and 1.4-(ie, conjugate addition) to α,β- unsaturated carbonyl compounds, using mechanisms to illustrate your answer. 5 marks
Please explain how to find the answers
Write the formulas of the conjugate bases of the acids below and name everything H2SO4 HNO3 HCI CH3COOH NHA HOCI Write the formulas of the conjugate acids of the bases below and name everything NH3 OH co,2 CH3COO HSO OCI For each of the neutral salts below, indicate whether their aqueous solutions are acid, basic, or neutral NH4CI KF Na2CO3 . In a 0.15 M solution of NaOH in water at 25 °C,...
please explain your answer
4. This question continues on the next page. For each of the following acid-base reactions: (0.3 pts ea = 3.0 pts) a. Predict the products that could form. b. Next to the products you draw, write either "Products not favored" or "Products favored." a. CH3OH + NaH → b. NaOH + CH3OH → C. KOH + (CH3)3COH → d. CH3OH + HI → dan gelen o e. HCECNa + CH3CH2OH → TH f. HCECH + CH3Li...
Circle the stronger BASE in each pair. No explanation, no
incomplete answers. I have 4 of these correct so I will know if
you’re getting them wrong.
3. Circle the stronger base in each pair. (0.2 pts ea = 2.0 pts) a. (CH3) 3COK vs. CH3OK b. HCECNa vs. CH3CH2ONa C. NaNH2 vs. HCECNa d. NacN vs. NaI e. NaHCO3 vs. NaOH f. NaOH vs. CoH5CO2Na g. C6H5COzNa vs. CoH5ONa h. CH3CO2Na vs. CH3ONa i. CH3ONa vs. NaH j. NH3...
please explain!
Problem 1 (30 pts) a) Name the compound shown below: CH3 CI b) Circle the alcohol that would dehydrate the fastest in H2SO4. به ما مبل c) Circle the products of the reaction below. پر20 1) KMnO4. KOH heat 2) HO* OH ) * ريم d) Circle the correct order of stability for the alkenes? V VV V V >c>b
I have the answers but can you explain please ?
Circle the stereoisomer that is the more stable compound? Explain your answer by drawing the most stable chair conformer of each compound using the partial chair structures below. Your equitorial and axial substituents must be unambiguous (if they're not, please label them).
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