The value of Kc < 1 for the given H 2 PO 4 − + F − ⇌ HF + HPO 4 2 − acid - base reaction has to be determined. Concept introduction: Conjugate acid-Base pairs: The acid donates the proton to form its conjugate base and the base accepts a proton to form its conjugate acid. When an acid is dissolved in water, the acid (HA) donates a proton to water to form a new acid (conjugate acid) and a new base (conjugate base). The pair of an Acid –Base differs by a proton called conjugated Acid-Base pair. In acid – base reaction, if the stronger acid produces the weaker acid which tells that the reaction favors the products, and the Kc value is greater than one ( Kc > 1 ) . If the weaker acid produces the stronger acid which tells that the reaction favors the reactants, and the Kc value is less than one ( Kc < 1 ) .
The value of Kc < 1 for the given H 2 PO 4 − + F − ⇌ HF + HPO 4 2 − acid - base reaction has to be determined. Concept introduction: Conjugate acid-Base pairs: The acid donates the proton to form its conjugate base and the base accepts a proton to form its conjugate acid. When an acid is dissolved in water, the acid (HA) donates a proton to water to form a new acid (conjugate acid) and a new base (conjugate base). The pair of an Acid –Base differs by a proton called conjugated Acid-Base pair. In acid – base reaction, if the stronger acid produces the weaker acid which tells that the reaction favors the products, and the Kc value is greater than one ( Kc > 1 ) . If the weaker acid produces the stronger acid which tells that the reaction favors the reactants, and the Kc value is less than one ( Kc < 1 ) .
The value of Kc < 1 for the given H2PO4− + F−⇌ HF + HPO42− acid - base reaction has to be determined.
Concept introduction:
Conjugate acid-Base pairs:
The acid donates the proton to form its conjugate base and the base accepts a proton to form its conjugate acid.
When an acid is dissolved in water, the acid (HA) donates a proton to water to form a new acid (conjugate acid) and a new base (conjugate base).
The pair of an Acid –Base differs by a proton called conjugated Acid-Base pair.
In acid – base reaction, if the stronger acid produces the weaker acid which tells that the reaction favors the products, and the Kc value is greater than one (Kc > 1). If the weaker acid produces the stronger acid which tells that the reaction favors the reactants, and the Kc value is less than one (Kc < 1).
(b)
Interpretation Introduction
Interpretation:
The value of Kc < 1 for the given CH3COO− + HSO4-⇌CH3COOH + SO42− acid - base reaction has to be determined.
Concept introduction:
Conjugate acid-Base pairs:
The acid donates the proton to form its conjugate base and the base accepts a proton to form its conjugate acid.
When an acid is dissolved in water, the acid (HA) donates a proton to water to form a new acid (conjugate acid) and a new base (conjugate base).
The pair of an Acid –Base differs by a proton called conjugated Acid-Base pair.
In acid – base reaction, if the stronger acid produces the weaker acid which tells that the reaction favors the products, and the Kc value is greater than one (Kc > 1). If the weaker acid produces the stronger acid which tells that the reaction favors the reactants, and the Kc value is less than one (Kc < 1).
CHEM2323
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Tt
PS CH03
Draw and name all monobromo derivatives of pentane, C5H11Br.
Problem 3-33
Name:
Draw structures for the following:
(a) 2-Methylheptane
(d) 2,4,4-Trimethylheptane
Problem 3-35
(b) 4-Ethyl-2,2-dimethylhexane
(e) 3,3-Diethyl-2,5-dimethylnonane
(c) 4-Ethyl-3,4-dimethyloctane
2
(f) 4-Isopropyl-3-methylheptane
KNIE>
Problem 3-42
Consider 2-methylbutane (isopentane). Sighting along the C2-C3 bond:
(a) Draw a Newman projection of the most stable
conformation.
(b) Draw a Newman projection of the least stable
conformation.
Problem 3-44
Construct a qualitative potential-energy diagram for rotation about the C-C bond of 1,2-dibromoethane.
Which conformation would you expect to be most stable? Label the anti and gauche conformations of 1,2-
dibromoethane.
Problem 3-45
Which conformation of 1,2-dibromoethane (Problem 3-44) would you expect to have the largest dipole
moment? The observed dipole moment of 1,2-dibromoethane is µ = 1.0 D. What does this tell you about the
actual conformation of the molecule?
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