The formula of acetylsalicylic acid is C9H8O4. And the gram formula mass of the molecule is 180 g/mol. So there is 325/180 = 1.8 mol. There is 6.02*10^23 molecules per mol. So the answer is 1.08 * 10^24 molecules.
Answer:
pH = 8.18
Explanation:
The weak base, X, reacts with HCl as follows:
X + HCl → HX⁺ + Cl⁻
<em>Where 1 mole of X with 1 mole of HCl produce 1 mole of HX⁺ (The conjugate acid of the weak base).</em>
Now, using H-H equation for bases:
pOH = pKb + log [XH⁺] / [X]
<em>Where pOH is the pOH of the buffer (pH = 14 -pOH)</em>
<em>pKb is -log Kb = 5.824</em>
<em>And [X] [HX⁺] are the molar concentrations of each specie</em>
Now, at the neutralization of the half of HX⁺, the other half is as X, that means:
[X] = [HX⁺]
And:
pOH = pKb + log [HX⁺] / [X]
pOH = 5.824 + log 1
pOH = 5.824
pH = 14-pOH
<h3>pH = 8.18</h3>
Answer:
by increasing temperature
Answer: <u>Endonuclease enzymes used in molecular biology that cut DNA at specified points.</u>
Explanation:
Enzymes are specific protein types which bind to a substrate within a reaction, to increase the rate of reaction within the solution- they speed up the rate of reaction.
Restriction enzymes are bacteria-derived enzymes; these make cuts on deoxyribonucleic acid molecules or DNA. These are also called restriction endonucleases. They are utilized in molecular biology for DNA cloning and sequencing and cut DNA into smaller pieces called fragments.
Restriction enzymes make directed cuts on DNA molecules. They precisely target sites on DNA to produce mostly identical or homogenous, discrete fragments of equal sizes, producing blunt or sticky ends. In order to do this, they recognize sequences of nucleotides that correspond with a complementary sequence on the endonuclease called restriction sites.
There are several kinds that may require cofactors (chemical or metallic compounds that aid in enzyme activity) :
- Type I: cleave far away from the recognition site; require ATP and SAMe S-Adenosyl-L-Methionine
- Type II: cleave near to the site; require Magnesium
- Type III: cleave near to the site; require ATP which is not hydrolysed but SAMe S-Adenosyl-L-Methionine is optional
- Type IV: cleavage targeted to DNA that have undergone post transcriptional modification through certain types of methylation (addition of a methyl group)
Waters boiling point is 100°C and 212°F