Answer: <span>A-Ce is oxidized because it is losing electrons and Cu is reduced because it is gaining electrons</span><span>.
</span>There are two reactions in the equation, oxidation and reduction. A molecule that oxidized will lose electrons while the molecule that reduced will gain electrons. In this case, Cu2+ changed into Cu which means its oxidation number reduced from +2 into 0. Ce oxidation number increased from 0 into +3
An iso pentane is an isomeric form of n-pentane. Isomers have same molecular formula but differ in the atomic arragement projected in 3D and the arrangement of atoms primarily resulting to a different set of properties. In this case, isopentane also has a molecular formula of an alkane <span>C5H12</span>
Answer:
3. 75.0%
Explanation:
2 ClO2(g) + F2(g) → 2 FClO2(g)
First order with respect to ClO2 and F2.
This means the rate equation is given as;
Rate = k [ClO2][F2]
When the initial concentrations of ClO2 and F2 are equal?
Let's assume an initial value of 1 for both reactants, so rate equation is given as;
Rate = k * 1 * 1 = k
The rate after 25% of the F2 has reacted is what percent of the initial rate?
The concentration left of F2 is 75% ( 100% - 25%) = 0.75
Concentration of ClO2 remains 1.
So rate equation is given as;
Rate = k * 1 * 0.75 = 0.75 k
Comparing 0.75k and k.
This means our answer is;
3. 75.0%
Answer:
Cell Membrane
The thin, flexible outer covering of a cell. It controls what enters and leaves a cell.
Explanation:
<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>