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Ch 09 Practice Problems - AP Chemistry

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Name:_______________________________ Date:_________________ Hr:____<br />

<strong>AP</strong> CHEMISTRY<br />

<strong>Ch</strong> 9 – Covalent Bonding: Orbitals<br />

PRACTICE PROBLEMS<br />

HYBRIDIZATION<br />

Suggested <strong>Problems</strong>: pp 418-420 15, 19, 27, 29<br />

28. For each of the following molecules or ions that contains sulfur, write the Lewis<br />

structure(s), predict the molecular geometry (including bond angles), and give the expected<br />

hybrid orbitals for sulfur (unless it has an expanded octet).<br />

Molecule or<br />

Ion<br />

Lewis Structure(s)<br />

Molecular<br />

Geometry<br />

Bond<br />

Angles<br />

Sulfur’s Hybrid<br />

Orbitals<br />

SO 2<br />

SO 3<br />

S 2 O 3<br />

2-<br />

SO 3<br />

2-<br />

SF 4<br />

SF 6<br />

F 3 S–SF<br />

SF 5<br />

+<br />

Page 1 of 3<br />

2013 mrluzio.com/apchem<strong>09</strong>


Name:_______________________________ Date:_________________ Hr:____<br />

<strong>AP</strong> CHEMISTRY<br />

<strong>Ch</strong> 9 – Covalent Bonding: Orbitals<br />

PRACTICE PROBLEMS<br />

30. The allene molecule has the following structural formula: H 2 C=C=CH 2 . Draw the Lewis<br />

structure for allene. Are all four hydrogen atoms in the same plane If not, what is their spatial<br />

relationship Explain.<br />

34. Hot and spicy foods contain molecules that stimulate pain-detecting nerve endings. Two<br />

such molecules are piperine and capsaicin:<br />

H<br />

d<br />

H O<br />

C a<br />

CH CH CH CH C<br />

H O<br />

b<br />

c O<br />

H<br />

H<br />

piperine<br />

H H<br />

H H<br />

H<br />

N f<br />

e<br />

H<br />

H H H H<br />

H 3 C<br />

H<br />

O<br />

O<br />

g<br />

H<br />

H<br />

CH 2<br />

H<br />

h<br />

N<br />

H<br />

O<br />

C<br />

CH 2<br />

(CH 2 ) 3 CH<br />

i j k<br />

capsaicin<br />

Piperine is the active compound in white and black pepper, and capsaicin is the active<br />

compound in chili peppers. The ring structures in piperine and capsaicin are shorthand<br />

notation. Each point where lines meet represents a carbon atom.<br />

a. Complete the structures for piperine & capsaicin showing all lone pairs of electrons.<br />

b. How many carbon atoms are sp, sp 2 , and sp 3 hybridized in each molecule<br />

Page 2 of 3<br />

2013 mrluzio.com/apchem<strong>09</strong><br />

CH<br />

CH<br />

CH 3<br />

l<br />

Piperine, sp: sp 2 : sp 3 : Capsaicin, sp: sp 2 : sp 3 :<br />

c. Which hybrid orbitals are used by the nitrogen atoms in each molecule<br />

Piperine:<br />

Capsaicin:<br />

d. Give approximate values for the bond angles marked a through l in the above<br />

structures.<br />

a: b: c: d: e: f: g: h: i: j: k: l:<br />

CH 3


Name:_______________________________ Date:_________________ Hr:____<br />

<strong>AP</strong> CHEMISTRY<br />

<strong>Ch</strong> 9 – Covalent Bonding: Orbitals<br />

PARAMAGNETISM AND DIAMAGNETISM<br />

PRACTICE PROBLEMS<br />

1. How can paramagnetic and diamagnetic substances be distinguished experimentally<br />

2. Which of the following atoms or ions are paramagnetic Justify your responses.<br />

a. H<br />

b. He<br />

c. Be<br />

d. B<br />

e. Cu<br />

f. Cu +<br />

g. Zn<br />

h. Br -<br />

i. Pb 4+<br />

j. U<br />

k. Element 118<br />

Page 3 of 3<br />

2013 mrluzio.com/apchem<strong>09</strong>

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