Answer: 625 kj/mol
Explanation:
As shown below this expression gives the activation energy of the reverse reaction:
EA reverse reaction = EA forward reaction + | enthalpy change |
1) The activation energy, EA is the difference between the potential energies of the reactants and the transition state:
EA = energy of the transition state - energy of the reactants.
2) The activation energy of the forward reaction given is:
EA = energy of the transition state - energy of [ NO2(g) + CO(g) ] = 75 kj/mol
3) The negative enthalpy change - 250 kj / mol for the forward reaction means that the products are below in the potential energy diagram, and that the potential energy of the products, [NO(g) + CO2(g) ] is equal to 375 kj / mol - 250 kj / mol = 125 kj/mol
4) For the reverse reaction the reactants are [NO(g) + CO2(g)], and the transition state is the same than that for the forward reaction.
5) The difference of energy between the transition state and the potential energy of [NO(g) + CO2(g) ] will be the absolute value of the change of enthalpy plus the activation energy for the forward reaction:
EA reverse reaction = EA forward reaction + | enthalpy change |
EA reverse reaction = 375 kj / mol + |-250 kj/mol | = 375 kj/mol + 250 kj/mol = 625 kj/mol.
And that is the answer, 625 kj/mol
<u>Answer:</u> The mass percent of hydrogen in methyl acetate is 8 %
<u>Explanation:</u>
The given chemical formula of methyl acetate is 
To calculate the mass percentage of hydrogen in methyl acetate, we use the equation:
Mass of hydrogen = (6 × 1) = 6 g
Mass of methyl acetate = [(3 × 12) + (6 × 1) + (2 × 16)] = 74 g
Putting values in above equation, we get:
Hence, the mass percent of hydrogen in methyl acetate is 8 %
Functional groups create reactive sites in molecules.
The polar part of a molecule that can hydrogen bond to water is said be hydrophilic.
Pi (π) bonds create active sites and will react with electron-deficient species.
A electronegative heteroatom like nitrogen, oxygen, or a halogen makes a carbon atom electrophilic.
(carbon will have less electronic density, which is attracted by the more electronegative heretoatoms, and it will tend to attract electron rich chemical species, and in this situation we say that the carbon atom is electrophilic).
The nonpolar part of a molecule that is not attracted to water is said to be hydrophobic.
A lone pair on a heteroatom makes it basic and nucleophilic.
(the heteroatom with the lone pair will tend to attract electron poor chemical species, and in this situation we say that the heteroatom is nucleophilic).
Answer:
1. Saturated hydrocarbons may be cyclic or acyclic molecules.
2. An unsaturated hydrocarbon molecule contains at least one double bond.
Explanation:
Hello,
In this case, hydrocarbons are defined as the simplest organic compounds containing both carbon and hydrogen only, for that reason we can immediately discard the third statement as ethylenediamine is classified as an amine (organic chain containing NH groups).
Next, as saturated hydrocarbons only show single carbon-to-carbon bonds and carbon-to-hydrogen bonds, they may be cyclic (ring-like-shaped) or acyclic (not forming rings), so first statement is true
Finally, since we can find saturated hydrocarbons which have single carbon-to-carbon and carbon-to-hydrogen bonds only and unsaturated hydrocarbons which could have double or triple bonds between carbons and carbon-to-hydrogen bonds, the presence of at least one double bond makes the hydrocarbon unsaturated.
Therefore, first and second statements are correct.
Best regards.
Answer:
The disadvantages of each of the given model of electron configuration have been mentioned below:
1). Dot Structures - They take up excess space as they do not display the electron distribution in orbitals.
2). Arrow and line diagrams make the counting of electrons and take up too much space.
3). Written Configurations do not display the electron distribution in orbitals and help in lose counting of electrons easily.
