Answer 1:
Isomers are compounds with same molecular formula but different structure formula. Isomers are classified into two types
a) Structural/configurational isomers
b) Stereo isomers
In structural/configurational isomers atom and functional groups are attached in different fashion. Structural isomers may have different functional groups. Structural isomers are further classified as chain isomers, position isomers and functional isomers. In case of stereo-isomers, compounds have same functional group, but different orientation in space. They also have difference activity towards polarized light.
Answer 2:
Hexane has a molecular formula of C6H14. It exhibits following structural isomers
a) hexane<span>,
b) 2-methylpentane
c)3-methylpentane
d) 2,2-dimethylbutane
e) 2,3-dimethylbutane
Thus, in all there are 5 isomers of hexane
Answer 3:
</span><span>Butane has two possible isomers but that decane has 75 possible isomers. This can be attributed to the fact that butane has 4 carbon atoms, while decane has 10 carbon atom. As the number of carbon atom increases, there are higher possible sites of linkage, in different fashion. Therefore, as number 69 of carbon atoms increases, number of different possible isomers increases.
Answer 4:
It has been observed that, though isomers have same molecular formula, but the have different boiling points. Infact, branched isomers have lower boiling point as compared to linear isomers. For example, hexane has boiling point = 69 oC, 2 methyl pentane has boiling point = 60 oC, 2,4, dimethyl butane has boiling point = 58 oC and 2,2 dimethyl butane has boiling point = 50 oC. Thus, it can be observed that branched isomers have lower boiling points as compared to linear isomers. This can be attributed to lower van der Waal's forces of interaction in branched isomers as compared to linear isomers.
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Answer:
because the number of constitutional confirmation , and geometric isomers goes up with each carbon atom added there are many more possible configurations and connectivities possible with decane , a 10 carbon chain , than with butane, a 4 carbon chain
Complete Question
You determine that it takes 26.0 mL of base to neutralize a sample of your unknown acid solution. The pH of the solution was 7.82 when exactly 13 mL of base had been added, you notice that the concentration of the unknown acid was 0.1 M. What is the pKa of your unknown acid?
Answer:
The pK_a value is 
Explanation:
From the question we are told
The volume of base is 
The pH of solution is 
The concentration of the acid is 
From the pH we can see that the titration is between a strong base and a weak acid
Let assume that the the volume of acid is 
Generally the concentration of base
Substituting value
When 13mL of the base is added a buffer is formed
The chemical equation of the reaction is
Now before the reaction the number of mole of base is
![No \ of \ moles[N_B] = C_B * V_B](https://tex.z-dn.net/?f=No%20%5C%20of%20%5C%20moles%5BN_B%5D%20%20%3D%20%20C_B%20%2A%20V_B)
Substituting value
Now before the reaction the number of mole of acid is
Substituting value
Now after the reaction the number of moles of base is zero i.e has been used up
this mathematically represented as
The number of moles of acid is
The pH of this reaction can be mathematically represented as
![pH = pK_a + log \frac{[base]}{[acid]}](https://tex.z-dn.net/?f=pH%20%20%3D%20pK_a%20%2B%20log%20%5Cfrac%7B%5Bbase%5D%7D%7B%5Bacid%5D%7D)
Substituting values
The volume is 2.23 liters of hydrogen gas.
<u>Explanation</u>:
moles of C = grams / molecular mass of C
= 1.04 g / 12.011 g/mol.
= 0.086
The ratio between C and H2 is 1 : 1
moles H2 = 0.086
V = nRT / p
= 0.086 x 0.08206 x 316 K / 1.0 atm
V = 2.23 L.
The enthalpy change for an exothermic reaction is negative because heat is being released, so that takes out two of the responses. Since energy is being released into the surroundings due to the exothermic reaction, the potential energy of the products is lower than that of the reactants. Energy is being put in to make the reaction occur, but then that energy is all being released into the surroundings thus a lower potential energy level for the products
