
Concept explainers
(a)
Interpretation:
The product of the following reaction has to be identified. Also, the acid and its conjugate base and the base and its conjugate acid for the following reaction have to be determined.
Concept Introduction:
In Bronsted–Lowry theory, acid is defined as a substance that donates a proton. In a solution, it dissociates to give
Base is defined as a substance that accepts a proton. In a solution, it dissociates to give
Brønsted–Lowry acid transfer a proton and form base as the other compound can accept a proton. This is called conjugate acid-base pair. In pair of conjugate acid and base, the acid form is protonated and the base form lost the proton.
Every base has a conjugate acid. They are related by loss or gain of proton. The expression for base and conjugate acid is as follows:
Every acid has a conjugate base. They are related by loss or gain of proton. The expression for conjugate base and acid is as follows:
The reaction mechanism in which proton is donated by a compound and accepted by the other compound is called a proton transfer reaction. It involves the transfer of protons between two species in chemical reaction.
(b)
Interpretation:
The product of the following reaction has to be identified. Also, the acid and it's conjugate base and the base and its conjugate acid for the following reaction have to be determined.
Concept Introduction:
Refer to part (a)
(c)
Interpretation:
The product of the following reaction has to be identified. Also, the acid and it's conjugate base and the base and its conjugate acid for the following reaction have to be determined.
Concept Introduction:
Refer to part (a)

Want to see the full answer?
Check out a sample textbook solution
Chapter 15 Solutions
Chemistry: Principles and Practice
- Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize 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_forward
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf 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_forward
- Indicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe 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_forward
- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate 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_forward
- Principles of Modern ChemistryChemistryISBN:9781305079113Author:David W. Oxtoby, H. Pat Gillis, Laurie J. ButlerPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
- Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningGeneral, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning





