The advantage of steam distillation over simple distillation is that the lower boiling point reduces decomposition of temperature -sensitive compounds.
The correct answer is H2SO3 I took the assignment already
Answer:
The new concentration is 0.125 M.
Explanation:
Given data:
Initial volume V₁ = 125.0 mL
Initial molarity M₁ = 0.150 M
New volume V₂ = 25 mL +125 mL = 150 mL
New concentration M₂ = ?
Solution:
M₁V₁ = M₂V₂
0.150 M × 125 mL = M₂ × 150 mL
M₂ = 0.150 M × 125 mL / 150mL
M₂ = 18.75 M.mL/150 mL
M₂ = 0.125 M
The new concentration is 0.125 M.
Answer:
15.4%
Explanation:
If Ka = 0.54 mM = 1.51x10⁻⁵
Then;
C₄H₈O₂ --------> C₄H₇O₂⁻ + H⁺
I 0.54x10⁻³ 0 0
E 0.54x10⁻³(1-x) 0.54x10⁻³x 0.54x10⁻³x
Recall that x is the percentage degree of dissociation
From the ICE table;
Ka = [C₄H₇O₂⁻] [ H⁺]/[C₄H₈O₂]
1.51x10⁻⁵=(0.54x10⁻³x) (0.54x10⁻³x)/ 0.54x10⁻³(1-x)
1.51x10⁻⁵ = 0.54x10⁻³x^2/1-x
1.51x10⁻⁵(1-x) = 0.54x10⁻³x^2
1.51x10⁻⁵ - 1.51x10⁻⁵x = 0.54x10⁻³x^2
Hence;
0.54x10⁻³x^2 + 1.51x10⁻⁵x - 1.51x10⁻⁵=0
x^2 + 0.028x - 0.028 = 0
Solving the quadratic equation here;
x = 0.154 or −0.182
Ignoring the negative result, x = 0.154
Hence, fraction of butanoic acid that is in the dissociated form in this solution = 15.4%
<span>You have to use a Newman projection to make sure that the H on C#2 is anti-coplanar with the Br on C#1. (Those are the two things that are going to be eliminated to make the alkene.)
My Newman projection looks like this when it's in the right configuration:
Front carbon (C#2) has ethyl group straight up, H down/left, and CH3 down/right
Back carbon (C#1) has H straight down, Ph up/left, and Br up/right.
Then when you eliminate the H from C#2 and the Br from C#1, you will have Ph and the ethyl group on the same side of the molecule, and you'll have the remaining H and CH3 on the same side of the molecule.
This is going to give you (Z)-2-methyl-1-phenyl-1-butene.</span>
