Answer:
1. Watt stream engine
2. McCormick reaper
3. Fulton steamboat
These are the correct answers.
Have A good day!! :)
In every direction guyz but conventionally it moves from higher potential to lower potential
According to the balanced equation of the reaction:
2C2H2 + 5O2 → 4CO2 + 2H2O
So we can mention all as liters,
A) as we see that 2 liters of C2H2 react with 5 liters of oxygen to produce 4 liters of CO4 and 2 liters of H2O
So, when we have 75L of CO2
and when we have 2 L of C2H2 reacts and gives 4 L of CO2
2C2H2 → 4CO2
∴ The volume of C2H2 required is:
= 75L / 2
= 37.5 L
B) and, when we have 75 L of CO2
and 4CO2 → 2H2O
∴ the volume of H2O required is:
= 75 L /2
= 37.5 L
C) and from the balanced equation and by the same way:
when 5 liters O2 reacts to give 4 liters of CO2
and we have 75 L of CO2:
5 O2 → 4 CO2
?? ← 75 L
∴ the volume of O2 required is:
= 75 *(5/4)
= 93.75 L
D) about the using of the number of moles the answer is:
no, there is no need to find the number of moles as we called everything in the balanced equation by liters and use it as a liter unit to get the volume, without the need to get the number of moles.
Answer:
See explanation and picture below
Explanation:
First, in the case of methyloxirane (Also known as propilene oxide) the mechanism that is taking place there is something similar to a Sn2 mechanism. Although a Sn2 mechanism is a bimolecular substitution taking place in only step, the mechanism followed here is pretty similar after the first step.
In both cases, the H atom of the HBr goes to the oxygen in the molecule. You'll have a OH⁺ in both. However, in the case of methyloxirane the next step is a Sn2 mechanism step, the bromide ion will go to the less substitued carbon, because the methyl group is exerting a steric hindrance. Not a big one but it has a little effect there, that's why the bromide will rather go to the carbon with more hydrogens. and the final product is formed.
In the case of phenyloxirane, once the OH⁺ is formed, the next step is a Sn1 mechanism. In this case, the bond C - OH⁺ is opened on the side of the phenyl to stabilize the OH. This is because that carbon is more stable than the carbon with no phenyl. (A 3° carbon is more stable than a 2° carbon). Therefore, when this bond opens, the bromide will go there in the next step, and the final product is formed. See picture below for mechanism and products.
Cp stands for specific heat.