<u>Answer:</u> The final pressure of the gas is 9.41 atm
<u>Explanation:</u>
To calculate the pressure of the gas, we use the equation given by ideal gas equation:

where,
P = pressure of the gas = ?
V = Volume of gas =
(Conversion factor:
)
n = Number of moles = 0.01 mol
R = Gas constant = 
T = temperature of the gas = ![300^oC=[300+273]K=573K](https://tex.z-dn.net/?f=300%5EoC%3D%5B300%2B273%5DK%3D573K)
Putting values in above equation, we get:

Hence, the final pressure of the gas is 9.41 atm
Answer:
HS+Na=>NaS+1/2H2(here HS- acts as an acid)
HS-. + HCl=> H2S(g)+ Cl-(here HS- acts as a base)
The graphics in the attachment is part of the question, which was incomplete.
Answer: Fr = 102N and angle of approximately 11°.
Explanation: From the attachment, it is observed that from the three forces acting on M, two are perpendicular. So to find them, we have to show their x- and y- axis components. From the graph:
Fx = 70+40-10 = 100
Fy = 40-20 = 20
Now, as the forces form a triangle, the totalforce is:
Fr = 
Fr = 
Fr = ≈ 102N
To determine the angle requested, we use:
arctg H = 
arctg H = 
H = tg 0.2 ≈ 11°.
Answer:
Your stomach lining also secretes hydrochloric acid, which creates the ideal conditions for the protein-digesting enzymes to work. The potent hydrochloric acid kills bacteria, protecting your body from harmful microbes which can enter your body in food.
Answer:
Here's what I get
Explanation:
You may have done a Williamson synthesis of guaifenesin by reacting guaiacol with 3-chloropropane-1,2-diol.
A. Mechanism
Step 1
NaOH converts guaiacol into a phenoxide ion.
Step 2
The phenoxide acts as the nucleophile in an SN2 reaction to displace the Cl from the alkyl halide.
B. Improve the yield
You probably carried out the reaction in ethanol solution — a polar protic solvent.
You might try doing the reaction in a polar aprotic solvent— perhaps DMSO.
A polar aprotic solvent does not hydrogen bond to nucleophiles, so they become stronger.
C. Another method of ether synthesis —dehydration of alcohols
Sulfuric acid catalyzes the conversion of primary alcohols to ethers.
This is also a nucleophilic displacement reaction.
Protonation of the OH converts it into a better leaving group.
Attack by a second molecule of alcohol forms the protonated ether.
A molecule of water then removes the proton.