Concept explainers
(a)
Interpretation:
Atomic orbitals which are used to form each
Concept Introduction:
Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.
Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.
Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.
Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,
(a)
Explanation of Solution
In the marked carbon atom, one s and three p orbital hybridize forming four
In the marked carbon atom, one s and two p orbital hybridize forming three
(b)
Interpretation:
Atomic orbitals which are used to form each
Concept Introduction:
Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.
Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.
Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.
Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,
(b)
Explanation of Solution
In the marked carbon atom, one s and two p orbital hybridize forming three
(c)
Interpretation:
Atomic orbitals which are used to form each
Concept Introduction:
Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.
Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.
Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.
Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,
(c)
Explanation of Solution
In the marked carbon atom, one s and two p orbital hybridize forming three
(d)
Interpretation:
Atomic orbitals which are used to form each
Concept Introduction:
Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.
Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.
Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.
Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,
(d)
Explanation of Solution
In the marked carbon atom, one s and two p orbital hybridize forming three
(e)
Interpretation:
Atomic orbitals which are used to form each
Concept Introduction:
Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.
Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.
Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.
Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,
(e)
Explanation of Solution
In the marked carbon atom, one s and one p orbital hybridize forming two
In the marked carbon atom, one s and two p orbital hybridize forming three
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Chapter 5 Solutions
Organic Chemistry
- Draw a three-dimensional representation of the valence orbitals and their bonding for compound CH2CHOH. Clearly show all valence electrons for each atom. Provide the following labels: atomic symbols, a code for each type of orbital used, a sigma bond, a pi bond and the molecular shape and approximate bond angles around the non-hydrogen atoms.arrow_forward3) How many electrons are delocalized in how many p-orbitals? Draw the most and second most stable resonance structures of the following compound. Order the structures by increasing stability. What is the partial charge distribution in the resonance hybrid?arrow_forwardHow does the valence bond description of a carboncarbon double bond account for cis trans isomers?arrow_forward
- What is the difference between the hybridization of carbon atoms' valence orbitals in saturated and unsaturated hydrocarbons?arrow_forward: The three bonds in the carbon-carbon triple bond in H-C≡C-H are:a _______ bond formed from _______ orbitalsa _______ bond formed from _______ orbitalsa _______ bond formed from _______ orbitalsarrow_forwardPart G. Molecules with Oxygen and Nitrogen. Organic molecules often contain the elements oxygen and nitrogen. Construct a model with the molecular formula C5H12O where the oxygen is bonded to one hydrogen. When a hydrogen is bonded to an oxygen or nitrogen, you need to draw that bond in a bond-line structure. Draw the bond-line structure of this model. What is the molecular geometry of oxygen in your structure? Draw three more constitutional isomers with the molecular formula C5H12O where the oxygen is bonded to one hydrogen. Structure Structure Structure Draw three more constitutional isomers with the molecular formula C5H12O where the oxygen is bonded to two carbon atoms. Structure Structure Structurearrow_forward
- Now write the condensed formulas for the following bond-line structures.arrow_forward6. Use VSEPR to predict the geometry and bond angle for each bolded atom in the following structures. HNO₂ H₂C=CHCI CH3CCHarrow_forward4. One of the resonance structures of "tropylium ion" (C7H7*) is shown below. It is planar and aromatic with Hückel number of p-n electrons where n=1. Draw all the other contributing resonance structures. (There are more than two.) Based on the “average" of the contributing resonance structures, how close does the average ring carbon get to its "octeť" in tropylium ion?arrow_forward
- What orbital does the lone pair on nitrogen sit in?arrow_forward4. Octatetraene, C8H10, is an 8-membered linear carbon chain with alternating single and double bonds. As a result, each carbon is left with an unhybridized p-orbital containing one electron. This problem will take you through steps to construct and fill the molecular orbital diagram for octatetraene based on the way these different p-orbitals can come together. a) The various molecular orbitals formed from octatetraene’s 8 unhybridized p-orbitals are shown on the next page. Draw the nodal planes for each molecular orbital. Hint: A nodal plane is a line through the molecule that denotes the sites of destructive interference. An example is shown below with ethylene. b) Based on the nodal planes, arrange the energy levels corresponding to the 8 molecular orbitals on the energy level diagram (label them using the numbering provided on the left side of the molecular orbitals) on the next page, in order of lowest to highest energy. c) Populate your molecular…arrow_forwardFor highlighted carbon atom , identify which atomic orbitals are used to form each σ bond and which are used to form each π bond.arrow_forward
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