Answer:
See explanation and picture below
Explanation:
First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.
In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.
In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.
Answer:
dna or diabeties can be separated
Molar mass Na2CO3 = 106 g/mole
Using dimensional analysis:
0.787 moles Na2CO3 x 106 g/mole Na2CO3 = g Na2CO3
Answer = 83.4 g Na2CO3
In general, we have this rate law express.:
![\mathrm{Rate} = k \cdot [A]^x [B]^y](https://tex.z-dn.net/?f=%5Cmathrm%7BRate%7D%20%3D%20k%20%5Ccdot%20%5BA%5D%5Ex%20%5BB%5D%5Ey)
we need to find x and y
ignore the given overall chemical reaction equation as we only preduct rate law from mechanism (not given to us).
then we go to compare two experiments in which only one concentration is changed
compare experiments 1 and 4 to find the effect of changing [B]
divide the larger [B] (experiment 4) by the smaller [B] (experiment 1) and call it Δ[B]
Δ[B]= 0.3 / 0.1 = 3
now divide experiment 4 by experient 1 for the given reaction rates, calling it ΔRate:
ΔRate = 1.7 × 10⁻⁵ / 5.5 × 10⁻⁶ = 34/11 = 3.090909...
solve for y in the equation
![\Delta \mathrm{Rate} = \Delta [B]^y](https://tex.z-dn.net/?f=%5CDelta%20%5Cmathrm%7BRate%7D%20%3D%20%5CDelta%20%5BB%5D%5Ey)

To this point,
![\mathrm{Rate} = k \cdot [A]^x [B]^1](https://tex.z-dn.net/?f=%5Cmathrm%7BRate%7D%20%3D%20k%20%5Ccdot%20%5BA%5D%5Ex%20%5BB%5D%5E1%20)
do the same to find x.
choose two experiments in which only the concentration of B is unchanged:
Dividing experiment 3 by experiment 2:
Δ[A] = 0.4 / 0.2 = 2
ΔRate = 8.8 × 10⁻⁵ / 2.2 × 10⁻⁵ = 4
solve for x for
![\Delta \mathrm{Rate} = \Delta [A]^x](https://tex.z-dn.net/?f=%5CDelta%20%5Cmathrm%7BRate%7D%20%3D%20%5CDelta%20%5BA%5D%5Ex)

the rate law is
Rate = k·[A]²[B]