Molecular Representations - Ch. 2 Flashcards
(23 cards)
What are the requirements for hydrogen bonding?
N, O, or F with a lone pair attached to an H
What is the important thing to remember when creating condensed structures?
the final structure must have the appropriate number of bonds for each element
Describe an aldehyde
C double bond O and C single bond H
Describe Carboxylic Acid
C double bond O, C single bond O single bond H
Describe an Ester
C double bond O, C single bond O, single bond R
Describe an Alkyne
R single bond C triple bond C single bond R
Describe Alkyl Halide
Carbon Chain with halogen at the end
Describe Alkane
All carbon carbon single bonds
Describe Alkene
Carbon chain with a double bond
What is the difference between a Ketone and Aldehyde
Ketone has a double bonded O in the middle and Aldehydes have O on the end
What are the keys to identifying functional groups?
- Locate all heteroatoms and pi bonds
- Classify each heteroatom as part of one functional group
What does it mean when an electron is delocalized?
spread out over more than one atom
What are two guidelines to drawing resonance structures?
- Draw electron pushing arrows from either lone pair electrons or pi bonds
- Draw arrows toward positive charges and away from negative charges
Define functional groups
characteristic group of atoms/bonds that possess a predictable chemical behavior
What do wedges indicate in a structure?
Groups coming out of the page
What do dashes indicate in a structure?
Group going behind the page
What is an acyclic compound?
Has no rings
What is a cyclic structure?
One ring
What is a bicyclic compound?
Has 2 rings
What is significant about resonance structures?
show the positive or negative charges are spread out over more than one location
What is the significance of delocalization?
stabilizing factor of molecules and ions
How do you know when a lone pair is delocalized?
It is located-in-the-p-orbital
List the 4 qualifications from most to least significant within resonance structures.
- greatest number of filled octets
- fewer formal charges
- negative charge on more electronegative element
- equally good Lewis structures are equivalent and contribute equally