Answer: a
Explanation: because an Arrhenius acid is a compound that increases the H + ion concentration in aqueous solution. An Arrhenius base is a compound that increases the OH − ion concentration in aqueous solution.
Finding percent composition is fairly easy. You only need to divide the mass of an element by the total mass of the compound. We can do this one element at a time.
First, let's find the total mass by using the masses of the elements given on the periodic table.
7 x 12.011 (mass of Carbon) = 84.077
5 x 1.008 (mass of Hydrogen) = 5.04
3 x 14.007 (mass of Nitrogen) = 42.021
6 x 15.999 (mass of Oxygen) = 95.994
Add all of those pieces together.
84.077 + 5.04 + 42.021 + 95.994 = 227.132 g/mol is your total. Since we also just found the mass of each individual element, the next step will be very easy.
Carbon: 84.077 / 227.132 = 0.37016 ≈ 37.01 %
Hydrogen: 5.04 / 227.132 = 0.022189 ≈ 2.22 %
Nitrogen: 42.021 / 227.132 = 0.185 ≈ 18.5 %
Oxygen: 95.994 / 227.132 = 0.42263 ≈ 42.26 %
You can check your work by making sure they add up to 100%. The ones I just found add up to 99.99, which is close enough. A small difference (no more than 0.03 in my experience) is just a matter of where you rounded your numbers.
Answer:
the reaction will shift towards the “heat”—shifts to the left
Explanation:
To summarize:
o If temperature increases (adding heat), the reaction will shift away from the “heat” term and go in the
endothermic direction.
o If temperature decreases (removing heat), the reaction will shift towards the “heat” term and go in the
exothermic direction.
o NOTE: The endothermic direction is always away from the “heat” term and the exothermic direction is
towards the “heat” term.
Therefore the reaction will shift towards the “heat”—shifts to the left
B) False- It has seven
A hexagon would have 6.
Answer:
Reagents: 1)
2)
, 
Mechanism: Hydroboration
Explanation:
In this case, we have a <u>hydration of alkene</u>s reaction. But, in this example, we have an <u>anti-Markovnikov reaction</u>. In other words, the "OH" is added in the least substituted carbon. Therefore we have to choose an anti-Markovnikov reaction: <u>"hydroboration"</u>.
The <u>first step</u> of this reaction is the addition of borane (
) to the double bond. Then in the <u>second step</u>, we have the deprotonation of the hydrogen peroxide, to obtain the peroxide anion. In the <u>third step</u>, the peroxide anion attacks the molecule produced in the first step to produce a complex compound in which we have a bond "
". In <u>step number 4</u> we have the migration of the C-B bond to oxygen. Then in <u>step number 5</u>, we have the attack of
on the
to produce an alkoxide. Finally, the water molecule produce in step 2 will <u>protonate</u> the molecule to produce the alcohol.
See figure 1
I hope it helps!