Variation in solubility of casein with pH has to be explained. Concept Introduction: Casein contains many carboxyl groups in the side chain. Carboxyl group ( COOH ) contains an acidic proton which can be easily donated. Carboxylic acid in basic medium will remove this proton and exists as stable carboxylate anion ( COO - ) . Water is polar solvent. Hence polar compounds will dissolve easily in water.
Variation in solubility of casein with pH has to be explained. Concept Introduction: Casein contains many carboxyl groups in the side chain. Carboxyl group ( COOH ) contains an acidic proton which can be easily donated. Carboxylic acid in basic medium will remove this proton and exists as stable carboxylate anion ( COO - ) . Water is polar solvent. Hence polar compounds will dissolve easily in water.
Definition Definition Group of atoms that shape the chemical characteristics of a molecule. The behavior of a functional group is uniform in undergoing comparable chemical reactions, regardless of the other constituents of the molecule. Functional groups aid in the classification and anticipation of reactivity of organic molecules.
Chapter 18, Problem 18.180P
(a)
Interpretation Introduction
Interpretation:
Variation in solubility of casein with pH has to be explained.
Concept Introduction:
Casein contains many carboxyl groups in the side chain. Carboxyl group (COOH) contains an acidic proton which can be easily donated. Carboxylic acid in basic medium will remove this proton and exists as stable carboxylate anion (COO-).
Water is polar solvent. Hence polar compounds will dissolve easily in water.
(b)
Interpretation Introduction
Interpretation:
Variation in solubility of histone with pH has to be explained.
Concept Introduction:
Histone contain -NH2 and =NH in its side chain. Nitrogen in these groups can accept proton and become positively charged species. In acidic medium, proton concentration will be more so -NH2 and =NH takes proton and becomes positively charged species.
Water is polar solvent. Hence polar compounds will dissolve easily in water.
The SN 1 mechanism starts with the rate-determining step which is the dissociation of the alkyl halide into a carbocation and a halide ion. The next step is
the rapid reaction of the carbocation intermediate with the nucleophile; this step completes the nucleophilic substitution stage. The step that follows the
nucleophilic substitution is a fast acid-base reaction. The nucleophile now acts as a base to remove the proton from the oxonium ion from the previous
step, to give the observed product. Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all nonzero formal
charges.
Cl:
Add/Remove step
G
Click and drag to start
drawing a structure.
Chapter 18 Solutions
Chemistry: The Molecular Nature of Matter and Change - Standalone book
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