(3.5mol)(24.106 g/1mol c6h6) =84.371 g C6H6
Answer: 
is the limiting reagent
Explanation:
To calculate the moles :
The balanced chemical reaction is :
According to stoichiometry :
1 moles of require = 2 moles of 
Thus 0.625 moles of will require=
of
Thus is the limiting reagent as it limits the formation of product and is the excess reagent as it is present more than the required amount.
El número de Avogadro es 6,022 x 10^23, y es el número de átomos que hay en un mol de dicho elemento. A su vez un mol es la cantidad de un elemento cuya masa en gramos coincide con el peso atómico.
Por tanto, 6,022 x 10^23 átomos del elemento tienen una masa en gramos igual a su peso atómico. Hacemos una regla de tres:
1 gramo -------- 1,5 x 10^22 átomos
x ------------------ 6,022 x 10^23 átomos
=> x = 40,1 gramos por mol del elemento.
De modo que su peso atómico es 40,1. Se trata del calcio.
Saludos.
Given:
<span>CS2 + 3O2 → CO2 + 2SO2
</span><span>114 grams of CS2 are burned in an excess of O2
</span>
moles CS2 = 114 g/76.143 g/mol → 114g * mol/76.143 g = 1.497 mol
<span>the ratio between CS2 and SO2 is 1 : 2 </span>
moles SO2 formed = 1.497 x 2 = 2.994 moles → 2nd option
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.
