Answer:
The formula for lithium acetate is CH3COOLi
Explanation:
The formula for lithium acetate is obtained by replacing the hydrogen atom bonding to the oxygen atom in acetic acid with Li as shown below:
CH3COOH + LiOH —> CH3COOLi + H2O
The pipette that accurately measures 0.8mL of fluid is P1000 micropipette.
It is given that:-
The volume of fluid = 0.8mL
We know that,
1 mL = 1000 microliter.
Hence,
0.8 mL = 0.8*1000 microliter = 800 microliter
We know that, a P1000 micropipette's volume ranges between 200 microliter to 1000 micro liter.
As,
200 < 800 < 100
Hence, P1000 micropipette is the right instrument.
The accuracy of this pipette decreases as volume decreases. Since the value 800 is near the maximum volume 1000 of the pipette, the accuracy of the pipette will be within a few percentages of the actual value.
To learn more about pipette, here:-
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Answer:
Percent yield = 90.8%
Explanation:
The reaction of Fe with S to produce FeS is:
Fe + S → FeS
<em>Where the moles of Fe added in excess of S are the moles of FeS</em>
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Now, percent yield is defined as 100 times the ratio between actual yield (13.8g of FeS) and theoretical yield (15.2g FeS):
Percent yield = 13.8g / 15.2g * 100
<h3>Percent yield = 90.8%</h3>
Answer: To calculate the enthalpy of combustion of acetylene, C2H2 , all you have to do is ... More specifically, you need to subtract from the sum of enthalpies of ... chemical reaction has 2 moles of C2H2 reacting to produce 2 moles of ... since the heat of combustion is expressed as energy per mole
Hi. You did not provide any response options. However, a PCR reaction proceeds as follows.
After the primers are added to the test tube containing the PCR components. This tube is placed in a device called a thermocycler. At that moment, the stage called denaturation will begin, where the thermocycler increases the temperature to the point of breaking the hydrogen bonds that hold the two strands of DNA together. The thermal cycler increases the temperature up to 96°C.
After that, the second step of the reaction begins. At that moment, the thermal cycler lowers the temperature to 55º - 65ºC, which is the ideal temperature for the primers to be able to attach themselves to the DNA strands, preparing them for the presence of the polymerase.
After that, the thermocycler raises the temperature to 72ºC, which is the ideal temperature for the DNA polymerase to work. At this stage, the DNA polymerase will use the DNA strand and the primer to build a new DNA strand, which will be annealed to the DNA strand used as a template.
These three steps will be repeated about 35 times, generating many copies of DNA.
