
(a)
Interpretation:
The structural effects in the given
Concept introduction:
Basicity of amines depends upon the nature of substituent present on the
(b)
Interpretation:
The structural effects in the given amines with their basicities are to be stated.
Concept introduction:
Basicity of amines depends upon the nature of substituent present on the aromatic ring. If substituent is electron withdrawing group then it has tendency to decrease the electron density and thus results in decrease in basicity of amines, whereas electron donating groups enhance the electron density and increases the basicity.
(c)
Interpretation:
The reason as to why the given compound is not only a stronger base but also a stronger hydroxide ion is to be explained.
Concept introduction:
Basicity of amines depends upon the nature of substituent present on the aromatic ring. If substituent is electron withdrawing group then it has tendency to decrease the electron density and thus results in decrease in basicity of amines, whereas electron donating groups enhance the electron density and increases the basicity.

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Chapter 19 Solutions
ORGANIC CHEMISTRY II LAB MANUAL>CUSTOM<
- Steps and explanation.arrow_forwardProvide steps and explanation please.arrow_forwardDraw a structural formula for the major product of the acid-base reaction shown. H 0 N + HCI (1 mole) CH3 N' (1 mole) CH3 You do not have to consider stereochemistry. ● • Do not include counter-ions, e.g., Na+, I, in your answer. . In those cases in which there are two reactants, draw only the product from 989 CH3 344 ? [Farrow_forward
- Assign these protonarrow_forwardCould you please solve the first problem in this way and present it similarly but color-coded or step by step so I can understand it better? Thank you!arrow_forwardCould you please solve the first problem in this way and present it similarly but color-coded or step by step so I can understand it better? Thank you!arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning

