Technically there is only one phase unless you account for a solution where you have a pure liquid with something dissolved in it. Unless you count aqueous as a phase which is just dissolved. Since you are in high school the answer you are looking for is one. <span />
Solids maintain their shape, whereas fluids do not because <span>the molecules in solids maintain a regular pattern and only vibrate, or move very slowly. The correct option among all the options that are given in the question is the last option or option "d". I hope the answer has come to your help.</span>
Answer:
Explanation:
Here, we want to convert J to cal
Mathematically:
Thus, to get our answer in cal, we divide the value given by 4.186
We have that as:
Answer:
The correct answer is option 3. Run a test reaction of crude oil with ocean water over time with Oil Spill Eater present
Explanation:
In any laboratory experiment, all the apparatus needed to carry out a particular experiment must be provided. In this case, our apparatus will be crude oil with ocean water and oil spill eater which is the enzyme used.
We can then run a test reaction of crude oil with ocean water over time with Oil Spill Eater present.
Answer:
Approximately 
, assuming that this acid is monoprotic.
Explanation:
Assume that this acid is monoprotic. Let 
denote this acid.
.
Initial concentration of without any dissociation:
![[{\rm HA}] = 0.730\; \rm mol \cdot L^{-1}](https://tex.z-dn.net/?f=%5B%7B%5Crm%20HA%7D%5D%20%3D%200.730%5C%3B%20%5Crm%20mol%20%5Ccdot%20L%5E%7B-1%7D)
.
After 
of that was dissociated, the concentration of both 
and 
(conjugate base of this acid) would become:
.
Concentration of in the solution after dissociation:
.
Let ![[{\rm HA}]](https://tex.z-dn.net/?f=%5B%7B%5Crm%20HA%7D%5D)
, ![[{\rm H}^{+}]](https://tex.z-dn.net/?f=%5B%7B%5Crm%20H%7D%5E%7B%2B%7D%5D)
, and ![[{\rm A}^{-}]](https://tex.z-dn.net/?f=%5B%7B%5Crm%20A%7D%5E%7B-%7D%5D)
denote the concentration (in 
or 
) of the corresponding species at equilibrium. Calculate the acid dissociation constant 
for , under the assumption that this acid is monoprotic:
![\begin{aligned}K_{\rm a} &= \frac{[{\rm H}^{+}] \cdot [{\rm A}^{-}]}{[{\rm HA}]} \\ &= \frac{(0.09125\; \rm mol \cdot L^{-1}) \times (0.09125\; \rm mol \cdot L^{-1})}{0.63875\; \rm mol \cdot L^{-1}}\\[0.5em]&\approx 1.30 \times 10^{-2} \end{aligned}](https://tex.z-dn.net/?f=%5Cbegin%7Baligned%7DK_%7B%5Crm%20a%7D%20%26%3D%20%5Cfrac%7B%5B%7B%5Crm%20H%7D%5E%7B%2B%7D%5D%20%5Ccdot%20%5B%7B%5Crm%20A%7D%5E%7B-%7D%5D%7D%7B%5B%7B%5Crm%20HA%7D%5D%7D%20%5C%5C%20%26%3D%20%5Cfrac%7B%280.09125%5C%3B%20%5Crm%20mol%20%5Ccdot%20L%5E%7B-1%7D%29%20%5Ctimes%20%280.09125%5C%3B%20%5Crm%20mol%20%5Ccdot%20L%5E%7B-1%7D%29%7D%7B0.63875%5C%3B%20%5Crm%20mol%20%5Ccdot%20L%5E%7B-1%7D%7D%5C%5C%5B0.5em%5D%26%5Capprox%201.30%20%5Ctimes%2010%5E%7B-2%7D%20%5Cend%7Baligned%7D)
.
