determine the total number of valence electrons; write the Lewis structure; give the electron pair Steric Number (or Coordination Number) of each central atom; indicate the type of hybrid orbitals used by each central atom; make a clear sketch of the structure; indicate all important bonds angles; describe the shape using one or two appropriate words such as linear, bent, trigonal planar, trigonal pyramidal, T-shaped, tetrahedral, square planar, see-saw, trigonal bipyramidal, o00 square pyramidal, octahedral, etc., for each central atom. a. BeH2 b. BC3 С. SO2 d. NH4+

Organic Chemistry: A Guided Inquiry
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Author:Andrei Straumanis
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Chapter3: Electron Orbitals
Section: Chapter Questions
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Using the table A-P I need to fill in the table in picture 2. I think this kinda absuses the one question rule so if you just do as many as you seem fair... Just further explanation a) is BeH2 and I need the formula, valence electrons, Lewis structure, S.N, hybrid orbitals, sketch with bomd angles and the shape thank you very much 

1.
a.
2.
3.
Procedure:
Note: The bulk of this work should be completed before you arrive at your scheduled lab.
No Data Sheet is submitted at the end of the lab period.
All work for this lab may be done in pencil.
1.
For each of the following molecules or ions (showing your work on pages 8(D) - 5 to 8(D) - 7):
determine the total number of valence electrons;
write the Lewis structure;
give the electron pair Steric Number (or Coordination Number) of each central atom;
indicate the type of hybrid orbitals used by each central atom;
make a clear sketch of the structure;
indicate all important bonds angles;
describe the shape using one or two appropriate words such as linear, bent, trigonal planar,
trigonal pyramidal, T-shaped, tetrahedral, square planar, see-saw, trigonal bipyramidal,
square pyramidal, octahedral, etc., for each central atom.
b.
BCI3
C.
SO2
a.
++HN
d.
NCI3
f.
g.
PBP5
h.
SF4
SH
i.
ICI3
PF6
ICI5
IF4-
n.
C2H4
O.
H3CCCH
CO2
Don't forget to indicate charge on Lewis structures by enclosing the structure in square
brackets, with the charge outside the bracket (upper right).
For each of the following make a labeled orbital diagram (on p. 8(D) - 8) showing how different
orbitals overlap to form bonds. Mark the bond angles on the diagram. Be sure to provide some
indication of the three dimensional shape for each.
B1SCK
a. CH3 - CH2 - CH2 - CH3
b. CH2 = CH - CH = CH - CI
c. H3C - C = C- CH = CH - Br
Make models (p. 8(D) - 8) of cis-1,2-dibromoethylene and trans-1,2-dibromoethylene. Sketch
these two structures. How can one be converted to another? Why does this not occur at room
temperature?
8(D) - 2
Transcribed Image Text:1. a. 2. 3. Procedure: Note: The bulk of this work should be completed before you arrive at your scheduled lab. No Data Sheet is submitted at the end of the lab period. All work for this lab may be done in pencil. 1. For each of the following molecules or ions (showing your work on pages 8(D) - 5 to 8(D) - 7): determine the total number of valence electrons; write the Lewis structure; give the electron pair Steric Number (or Coordination Number) of each central atom; indicate the type of hybrid orbitals used by each central atom; make a clear sketch of the structure; indicate all important bonds angles; describe the shape using one or two appropriate words such as linear, bent, trigonal planar, trigonal pyramidal, T-shaped, tetrahedral, square planar, see-saw, trigonal bipyramidal, square pyramidal, octahedral, etc., for each central atom. b. BCI3 C. SO2 a. ++HN d. NCI3 f. g. PBP5 h. SF4 SH i. ICI3 PF6 ICI5 IF4- n. C2H4 O. H3CCCH CO2 Don't forget to indicate charge on Lewis structures by enclosing the structure in square brackets, with the charge outside the bracket (upper right). For each of the following make a labeled orbital diagram (on p. 8(D) - 8) showing how different orbitals overlap to form bonds. Mark the bond angles on the diagram. Be sure to provide some indication of the three dimensional shape for each. B1SCK a. CH3 - CH2 - CH2 - CH3 b. CH2 = CH - CH = CH - CI c. H3C - C = C- CH = CH - Br Make models (p. 8(D) - 8) of cis-1,2-dibromoethylene and trans-1,2-dibromoethylene. Sketch these two structures. How can one be converted to another? Why does this not occur at room temperature? 8(D) - 2
2. You may complete this entiré réport in pen
Formula
Valence
Lewis
S.N.
Hybrid
Sketch with Bond
Shape
Electrons
Structure
Angles
Orbitals
Transcribed Image Text:2. You may complete this entiré réport in pen Formula Valence Lewis S.N. Hybrid Sketch with Bond Shape Electrons Structure Angles Orbitals
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