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The sp2hybrid atomic orbitals have the following general form:

role="math" localid="1663746599823" ϕ1=13ϕs+2pxϕ2=13ϕs-2px+pyϕ3=13ϕs-2px-py

where, Φs,Φpxandrole="math" localid="1663746751426" Φpyrepresent orthonormal (normalized and orthogonalized) atomic orbitals. Calculate the values of Aand B.

Short Answer

Expert verified

A=16andB=12

The probability of finding a particle is one.

Step by step solution

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01

Find A

Calculate the value of A as follows.

132+4A2=1A2=212A=16

02

Find B

Calculate the value of B as follows.

132+A2+B2=1B=1-16-13B=12

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Most popular questions from this chapter

Consider the molecular orbital electron configurations forN2 , N2+, and N2-. For each compound or ion, fill in the table below with the correct number of electrons in each molecular orbital.

MO

N2


role="math" localid="1663764752673" N2+


role="math" localid="1663764766917" N2-

role="math" localid="1663764800461" σ2p*

role="math" localid="1663764811953" π2p*

role="math" localid="1663764822519" σ2p

role="math" localid="1663764834336" π2p

role="math" localid="1663764966754" σ2s*

role="math" localid="1663764978558" σ2s

Draw the Lewis structures, predict the molecular structures, and describe the bonding (in terms of the hybrid orbitals for the central atom) for the following.

a.XeO3b.XeO4c.XeOF4d.XeOF2e.XeO3F2

For each of the following chemical formulas, an NMR spectrum is described, including relative overall areas (intensities) for the various signals given in parentheses. Draw the structure of a compound having the specific formula that would give the described NMR spectrum. Hint: All of these formulas represent organic compounds. Lewis structures for organic compounds typically have all atoms in the compound with a formal charge of zero. This is the case in this problem.)

a.C2H3Cl3;NMRhas one singlet signal.

b.C3H6Cl2;NMRhas a triplet (4) and a quintet (2) signal.

c.C3H6O2; NMR has a singlet (1), a quartet (2), and a triplet (3)signal.

d.C5H10O; NMR has a heptet (1), a singlet (3), and a doublet (6) signal.

e.C3H6O;NMRhas a triplet (3), a quintet (2), and a triplet (1) signal.

Hot and spicy foods contain molecules that stimulate pain-detecting nerve endings. Two such molecules are piperine and capsaicin

Piperine is the active compound in white and black pepper, and capsaicin is the active compound in chili peppers. The ring structures in piperine and capsaicin are short-hand notation. Each point where lines meet represents a carbon atom.

a. Complete the Lewis structures for piperine and capsaicin, showing all lone pairs of electrons.

b. How many carbon atoms are sp, sp2, and sp3 hybridized in each molecule?

c. Which hybrid orbitals are used by the nitrogen atoms in each molecule?

d. Give approximate values for the bond angles marked a through l in the above structures.

Draw the Lewis structures for SeO2, PCl3, NNO, COS, and PF3. Which of the compounds are polar? Which of the compounds exhibit at least one bond angle that is approximately 120 degrees? Which of the compounds exhibit hybridization by the central atom? Which of the compounds have a linear molecular structure?

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