Block 1: Foundations Flashcards
What is the charge of the more electronegative element?
More negative
Why are double bonds more readily polarised?
Due to the relative mobility it pi electrons
What is sp3?
A carbon with 4 atoms attached
Which molecules have a higher boiling point?
Those with an increased molecular size
What do more functional groups/polar bonds do to boiling point?
Correlates with a higher boiling point
What is a primary alcohol?
When the alcohol is attached to a carbon connected to one other carbon
What is a secondary (2•) alcohol?
When the OH is attached to a carbon attached to two other carbons
What is a tertiary (3•) carbon?
When the OH group is attached to a carbon attached to three other carbons
(Also used for alkyl halides)
What is an ortho- aromatic compound?
X2 Cl are in the 1,2 position
What is a meta aromatic compound?
X2 Cl are in the 1,3 position
What is a para aromatic compound?
X2 Cl are in the 1,4 position
What is a constitutional isomer?
Different sequence of bonds
What is a stereoisomer?
Different arrangement of groups in space
What is a conformational isomer?
Differ by rotation around a single bond
What is a configuration so isomer?
Interconversion requires breaking bonds
What are enantiomers?
Non-super imposable mirror images
What are diastomers?
Non mirror images
What is the formula for a molecular formula with no rings and only single bonds?
Cn H2n+2
What is the formula for a molecule that must contain either one double bond or ring?
CnH2n
Formula for double bonds equivalents?
1/2 (2xcarbon + (nitrogen) - hydrogen + 2) = number of double bonds
What is a staggered Newman projection?
Not blocking each other
What is an eclipsed Newman projection?
The C-C block each other
What is an anti Newman projection?
When it’s staggered and the largest group are furthest away (and most stable)
What is a gauche Newman projection?
When its staggered and the largest groups are closest together