(a)
Interpretation:
To draw resonance structure for the conjugate base of given set of compounds when it is treated with sodium ethoxide.
Concept introduction:
A conjugate base is formed when an base abstract the acidic proton from a compound to form an ion. The charge on the ion can undergo delocalization within the molecule to form resonance stabilized conjugate base. The more the charge is delocalized, the more the conjugate base is stable which inturn indicates that the compound is more acidic.
To draw : The resonance structure of conjugate base formed
(b)
Interpretation:
To draw resonance structure for the conjugate base of given set of compounds when it is treated with sodium ethoxide.
Concept introduction:
A conjugate base is formed when an base abstract the acidic proton from a compound to form an ion. The charge on the ion can undergo delocalization within the molecule to form resonance stabilized conjugate base. The more the charge is delocalized, the more the conjugate base is stable which inturn indicates that the compound is more acidic.
To draw : The resonance structure of conjugate base formed
(c)
Interpretation:
To draw resonance structure for the conjugate base of given set of compounds when it is treated with sodium ethoxide.
Concept introduction:
A conjugate base is formed when an base abstract the acidic proton from a compound to form an ion. The charge on the ion can undergo delocalization within the molecule to form resonance stabilized conjugate base. The more the charge is delocalized, the more the conjugate base is stable which inturn indicates that the compound is more acidic.
To draw : The resonance structure of conjugate base formed
Want to see the full answer?
Check out a sample textbook solution
Chapter 21 Solutions
EBK ORGANIC CHEMISTRY-PRINT COMPANION (
- Synthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- If possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forward
- We mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forward
- Indicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are mixed with sodium ethoxide in ethanol.arrow_forward
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY