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5. Circle all of the bases below that can be used successfully...
please explain your answers 6. Circle all of the bases below that can be used successfully to deprotonate phenol (C...
please explain your answers
6. Circle all of the bases below that can be used successfully to deprotonate phenol (CsHsOH). (0.2 pts) a. KOH b. NHa c. NaHCO3 d. 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.
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...
Circle the stronger base in each pair 3. Circle the stronger base in each pair. (0.2 pts ea = 2.0 pts) a. (CH3) 3CO...
Circle the stronger base in each pair
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 vs. CH3CO2Na
please explain your answers 4. This question continues on the next page. For each of the...
please explain your answers
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 CHO Na + H₂ products favored b. NaOH + CH3OH → CH₂O N2 + H₂O products favored C. KOH + (CH3)3COH (CH3), COK + H20 products favored d. CH₃OH...
please answer all the parts The following compounds can all behave as bases: 4. NANH2 NAOH...
please answer all the parts
The following compounds can all behave as bases: 4. NANH2 NAOH CH3CH2OH CH3CH2NH2 NH2 For each compound, draw its conjugate acid. а. Rank the acids in order of increasing basicity. Explain your ranking. 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
6. Circle all of the bases below that can be used successfully to deprotonate phenol (CsHsOH). (0.2 pts) a. KOH b. NHa c. NaHCO3 d. 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.
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...
Circle the stronger base in each pair
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 vs. CH3CO2Na
please explain your answers
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 CHO Na + H₂ products favored b. NaOH + CH3OH → CH₂O N2 + H₂O products favored C. KOH + (CH3)3COH (CH3), COK + H20 products favored d. CH₃OH...
please answer all the parts
The following compounds can all behave as bases: 4. NANH2 NAOH CH3CH2OH CH3CH2NH2 NH2 For each compound, draw its conjugate acid. а. Rank the acids in order of increasing basicity. Explain your ranking. 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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