
(a)
Interpretation:
Lewis structure of
Concept-Introduction:
Lewis structure:
Electron dot structure also known as Lewis dot structure represents the number of valence electrons of an atom or constituent atoms bonded in a molecule. Each dot corresponds to one electron.
(b)
Interpretation:
MO diagrams of
Concept-Introduction:
Molecular orbital (MO) theory: It is a method for determining molecular structure in which electrons are not assigned to individual bonds between atoms, but are treated as moving under the influence of the nuclei in the whole molecule.
According to this theory there are two types of orbitals,
- (1) Bonding orbitals
- (2) Antibonding orbitals
Electrons in molecules are filled in accordance with the energy; the anti-bonding orbital has more energy than the bonding orbitals.
The electronic configuration of oxygen molecule
The * represent the antibonding orbital
Orbital diagram represents each orbital with a box, with orbital’s in the same subshell in connected boxes, electrons are shown as arrows in the boxes, pointing up or down to indicate their spins.
Bond order: It is the measure of number of electron pairs shared between two atoms.
Bond length is inversely proportional to the bond order.
If two or more different chemical species having same number of valence electrons are known as isoelectronic species.

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Chapter 14 Solutions
Chemistry: The Molecular Nature of Matter and Change
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- Problem 6-17 Look at the following energy diagram: Energy Reaction progress (a) Is AG for the reaction positive or negative? Label it on the diagram. (b) How many steps are involved in the reaction? (c) How many transition states are there? Label them on the diagram. Problem 6-19 What is the difference between a transition state and an intermediate? Problem 6-21 Draw an energy diagram for a two-step reaction with Keq > 1. Label the overall AG°, transition states, and intermediate. Is AG° positive or negative? Problem 6-23 Draw an energy diagram for a reaction with Keq = 1. What is the value of AG° in this reaction?arrow_forwardProblem 6-37 Draw the different monochlorinated constitutional isomers you would obtain by the radical chlorination of the following compounds. (b) (c) Problem 6-39 Show the structure of the carbocation that would result when each of the following alkenes reacts with an acid, H+. (a) (b) (c)arrow_forwardPlease draw the major product of this reaction. Ignore inorganic byproducts and the carboxylic side productarrow_forward
- predict the product formed by the reaction of one mole each of cyclohex-2-en-1-one and lithium diethylcuprate. Assume a hydrolysis step follows the additionarrow_forwardPlease handwriting for questions 1 and 3arrow_forwardIs (CH3)3NHBr an acidic or basic salt? What happens when dissolved in aqueous solution? Doesn't it lose a Br-? Does it interact with the water? Please advise.arrow_forward
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