Answer:
1.- Theoretical yield is 1.64 g of aspirin
2.- %Yield is 75.6%
Explanation:
The theoretical yield of aspirin could be calculated by the molar relation between anhydride acetic and salicylic acid which is 1:1. It means that the reaction of one mole of anhydride acetic with one mole of salicylic acid will produce 1 mole of aspirin and one mole of acetic acid.
It is possible to calculated the number of moles using moles=grams/molar mass. in the attached figure we can see the molar mass of each compound.
The number of moles of anhydride acetic can be calculated using the density and the volumen.
g=(1.08 g/mL)*(2.90 mL)=3.13 g of anhydride
moles= 3.13 g/(102.09 g/mol)= 0.031 moles of anhydride acetic
The same for salicylic acid and we have:
moles= 1.23g/ (138.12 g/mol)= 0.0090 moles of salicylic acid
There is not 1:1 relation between this two compounds because there is much more anhydride acetic than salicylic acid, so the reaction is limited by the 0.0090 moles of salicylic acid which produce 0.0090 moles of aspirin.
g= moles*molar mass
Theoretical yield of aspirin= (0.009 moles)*(182.13 g/mol)= 1.64 g
The percent yield of aspirin for the reaction can be calculated using the nex formula:
%yield= ((real yield)/(theoretical yield))*100
The real yield was 1.24 g of aspirin
%Yield=(1.24g/1.64)*100=75.6%
To determine the theoretical yield of aspirin, calculate the moles of acetic anhydride and salicylic acid, use the balanced equation to find the moles of aspirin, and convert to grams. The percent yield is calculated by dividing the actual yield by the theoretical yield and multiplying by 100.
To determine the theoretical yield of aspirin, we need to first calculate the number of moles of acetic anhydride and salicylic acid. Then, we use the balanced equation to find the number of moles of aspirin produced. Finally, we convert the moles of aspirin to grams using its molar mass. The percent yield is calculated by dividing the actual yield by the theoretical yield and multiplying by 100.
Step 1: Calculate the moles of acetic anhydride
2.90 mL × 1.08 g/mL = 3.132 g
Moles of acetic anhydride = mass / molar mass = 3.132 g / 102.09 g/mol = 0.0307 mol
Step 2: Calculate the moles of salicylic acid
Moles of salicylic acid = mass / molar mass = 1.23 g / 138.12 g/mol = 0.0089 mol
Step 3: Use the balanced equation to find the moles of aspirin produced
According to the balanced equation: 1 mol of acetic anhydride reacts with 1 mol of salicylic acid to produce 1 mol of aspirin
Since the moles of acetic anhydride and salicylic acid are the same, the moles of aspirin produced = 0.0089 mol
Step 4: Calculate the theoretical yield of aspirin in grams
The molar mass of aspirin is 180.16 g/mol
Theoretical yield of aspirin = moles of aspirin × molar mass of aspirin = 0.0089 mol × 180.16 g/mol = 1.61 g
Step 5: Calculate the percent yield of aspirin
Percent yield = (actual yield / theoretical yield) × 100
Percent yield = (1.24 g / 1.61 g) × 100 = 77.0%
#SPJ6
b. gas pressure.
c. a decrease in volume.
d. an overall loss of energy.
Raising the temperature of a gas will increase its pressure if the volume of the gas
a. and the number of particles are increased.
b. is increased, but the number of particles is constant.
c. and the number of particles are constant.
d. is constant, but the number of particles is reduced.
In less scientific words
For number 1 is GAS PRESSURE
And number 2 is TEMPERATURE
The compound that is a saturated hydrocarbon is CH3CH2OH. The answer is letter A. A saturated hydrocarbon has only one single bond between the carbon atoms. The compound that is an unsaturated hydrocarbon is CHCH. The answer is letter D.
Answer:
Theory
Explanation:
Answer:
The rubber becomes brittle and can break in your hand. The explanation for why this happens concerns cross-linking bonds. Ultra-violet light from the sun provides the polymer molecules with the activation energy they need to be able to form more cross-links with other chains.
If excessively excessive cross-links are formed in rubber, it becomes overly rigid and brittle, hampering its natural elasticity and strength. The increase in cross-links restricts the moving of the polymer chains, undermining the effectiveness of the rubber in many applications.
The formation of cross-links in rubber significantly affects its properties. In the case where too many cross-links are formed, the rubber is likely to become overly rigid and brittle. This is because the cross-links restrict the movement of the polymer chains, which reduces flexibility and elasticity. As a result, too many cross-links can compromise the usefulness of rubber for many applications, which require its natural elasticity and strength. For example, in a rubber band, if too many cross-links were formed, then it would be less stretchy and snap more easily when stretched.
#SPJ2
Explanation:
1s 2s 2p
1s 2s 2p1s2 2s1
1s 2s 2p1s2 2s1 2 1 1
1s 2s 2p1s2 2s1 2 1 11s2 2s2