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(a)
Interpretation: The formula of conjugate acid of base dimethylamide should be written.
Concept introduction: In accordance with Bronsted definition, an acid act as proton donor and a base can act as proton acceptor. Thus, in a typical acid-base reaction, the fundamental principle is a lone pair of base reaches out for an acidic proton. Similarly, curved arrows are used for departing conjugate base. After deprotonation, the species left with negative charge is refers as conjugate base of acid while the other with positive charge is termed conjugate acid of given base. For example:
The strength of various conjugate acid-base pairs varies inversely to one another; the strong acid has weak conjugate base and strong base has weak conjugate acid and vice-versa.
(b)
Interpretation: The formula of conjugate acid of sulfide should be written.
Concept introduction: In accordance with Bronsted definition, an acid act as proton donor and a base can act as proton acceptor. Thus, in a typical acid-base reaction, the fundamental principle is a lone pair of base reaches out for an acidic proton. Similarly, curved arrows are used for departing conjugate base. After deprotonation, the species left with negative charge is refers as conjugate base of acid while the other with positive charge is termed conjugate acid of given base. For example:
The strength of various conjugate acid-base pairs varies inversely to one another; the strong acid has weak conjugate base and strong base has weak conjugate acid and vice-versa.
(c)
Interpretation: The formula of conjugate acid of ammonia should be written.
Concept introduction: In accordance with Bronsted definition, an acid act as proton donor and a base can act as proton acceptor. Thus, in a typical acid-base reaction, the fundamental principle is a lone pair of base reaches out for an acidic proton. Similarly, curved arrows are used for departing conjugate base. After deprotonation, the species left with negative charge is refers as conjugate base of acid while the other with positive charge is termed conjugate acid of given base. For example:
The strength of various conjugate acid-base pairs varies inversely to one another; the strong acid has weak conjugate base and strong base has weak conjugate acid and vice-versa.
(d)
Interpretation: The formula of conjugate acid of acetone should be written.
Concept introduction: In accordance with Bronsted definition, an acid act as proton donor and a base can act as proton acceptor. Thus, in a typical acid-base reaction, the fundamental principle is a lone pair of base reaches out for an acidic proton. Similarly, curved arrows are used for departing conjugate base. After deprotonation, the species left with negative charge is refers as conjugate base of acid while the other with positive charge is termed conjugate acid of given base. For example:
The strength of various conjugate acid-base pairs varies inversely to one another; the strong acid has weak conjugate base and strong base has weak conjugate acid and vice-versa.
(e)
Interpretation: The formula of conjugate acid of
Concept introduction: In accordance with Bronsted definition, an acid act as proton donor and a base can act as proton acceptor. Thus, in a typical acid-base reaction, the fundamental principle is a lone pair of base reaches out for an acidic proton. Similarly, curved arrows are used for departing conjugate base. After deprotonation, the species left with negative charge is refers as conjugate base of acid while the other with positive charge is termed conjugate acid of given base. For example:
The strength of various conjugate acid-base pairs varies inversely to one another; the strong acid has weak conjugate base and strong base has weak conjugate acid and vice-versa.
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Chapter 2 Solutions
ORGANIC CHEMISTRY (LL)-PACKAGE
- On what basis are Na and Nb ranked against each other?arrow_forwardStep 1: add a curved arrow. Select Draw Templates More / " C H Br 0 Br : :o: Erase H H H H Q2Q Step 2: Draw the intermediates and a curved arrow. Select Draw Templates More MacBook Air / " C H Br 0 9 Q Erase 2Qarrow_forwardO Macmillan Learning Question 23 of 26 > Stacked Step 7: Check your work. Does your synthesis strategy give a substitution reaction with the expected regiochemistry and stereochemistry? Draw the expected product of the forward reaction. - - CN DMF MacBook Air Clearly show stereochemistry. Questionarrow_forward
- NH2 1. CH3–MgCl 2. H3O+ ? As the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule with a new C - C bond as its major product: If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. If the major products of this reaction won't have a new C - C bond, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. This reaction will not make a product with a new C - C bond. Х ☐: Carrow_forwardPredict the major products of this organic reaction. If there will be no major products, check the box under the drawing area instead. No reaction. : + Х è OH K Cr O 2 27 2 4' 2 Click and drag to start drawing a structure.arrow_forwardLaminar compounds are characterized by havinga) a high value of the internal surface of the solid.b) a high adsorption potential.arrow_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 Learning
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