Answer:
The value is 
Explanation:
From the question we are told that

The initial volume of the fluorocarbon gas is 
The final volume of the fluorocarbon gas is
The initial temperature of the fluorocarbon gas is 
The final temperature of the fluorocarbon gas is 
The initial pressure is 
The final pressure is 
Generally the equation for adiabatically reversible expansion is mathematically represented as
![T_2 = T_1 * [ \frac{V_1}{V_2} ]^{\frac{R}{C_v} }](https://tex.z-dn.net/?f=T_2%20%3D%20%20T_1%20%20%2A%20%5B%20%5Cfrac%7BV_1%7D%7BV_2%7D%20%5D%5E%7B%5Cfrac%7BR%7D%7BC_v%7D%20%7D)
Here R is the ideal gas constant with the value

So
=> 
Generally adiabatic reversible expansion can also be mathematically expressed as

=>
=> 
=>
So

=> 
Answer:
25°C
Explanation:
Combined Gas Law (P₁V₁)/T₁ = (P₂V₂)/T₂
(0.947 atm)(150 mL)/25°C = (0.987 atm)(144mL)/T₂
5.682 = 142.128/T₂
T₂ = 142.128/5.682
T₂ = 25.0137272756°C = 25°C
The structures of the isomers and the m/z values of their peaks are not given in the question. The complete question is provided in the attachment
Answer:
Compound 2 (2,5-dimethylhexane) will not have the peaks at 29 and 85 m/z
Explanation:
The fragmentation of molecules by electron ionization of mass spectrometer occurs according to Stevenson's Rule, which states that "The most probable fragmentation is the one that leaves the positive charge on the fragment with the lowest ionization energy". This is much like the Markovnikov's Rule in organic chemistry which has predicted the formation of most stable carbocation and the addition of hydrogen halide to it.
The mass spectra of compound 1 (2,4-dimethylhexane) will contain all the m/z values mentioned in the question. Each peak indicate towards homologous series of fragmentation product of the compound 1. The first peak can be attributed to ethyl carbocation (m/z = 29), with the increase of 14 units the next peak indicates towards propyl carbocation (m/z = 43) and onwards until molecular ion peak of 114 m/z.
Compound 2 (2,5-dimethylhexane) structure shows that the cleavage of C-C bond will not yield a stable ethyl and hexyl carbocation. Hence, no peaks will be observed at 29 and 85 m/z. The absence of these two peaks can be used to distinguish one isomer from the other.
1.00mol is the correct answer
Reactant: carbon dioxide and sodium phenoxide
product: sodium salicylate