You would find the highest pressure at the bottom
Answer:
The answer is aluminum foil.
Answer:
The four resonance structures of the phenoxide ion are shown in the image attached
The conjugate base of cyclohexanol has only one resonance contributor, while
the conjugate base of phenol has four resonance contributors.
Explanation:
In organic chemistry, it is known that structures are more stable if they possess more resonance contributors. The greater the number of contributing canonical structures, the more stable the organic specie. Since the phenoxide ion has four contributing canonical structures, it is quite much more stable than cyclohexanol having only one contributing structure to its conjugate base. Hence the PKa(acid dissociation constant) of phenol is lesser than that of cyclohexanol. The conjugate base of phenol is stabilized by resonance.
Answer:
Identical
Explanation:
Both compounds are identical. If you rotate the compound on the left 60 degree anticlockwise you will get the compound on the right.
These are not isomers of each other because they have same structural and molecular formulas.
Also, they are related to each other because they are the same
Answer:
The method is accurate in the calculation of the 
Explanation:
As a first step we have to calculate the <u>average concentration </u>of
find it by the method.

Then we have to find the<u> standard deviation:</u>

For the confidence interval we have to use the formula:
μ=Average±
Where:
t=t student constant with 95 % of confidence and 5 data=2.78
μ=
± 
upper limit: 0.84
lower limit: 0.75
If we compare the limits of the value obtanied by the method (Figure 1 Red line) with the reference material (Figure 1 blue line) we can see that the values obtained by the method are within the values suggested by the reference material. So, it's method is accurate.