GB1: Chapter 4 Flashcards
Organic chemistry
study of compounds containing carbon (organic compounds)
Atom’s valence
number of covalent bonds atom can form
hydrocarbons
organic molecules consisting only carbon and hydrogen
atoms of hydrogen are attached to the carbon skeleton wherever electrons can covalently bond
isomers and types
compounds that have same numbers of atoms of same elements but different structures and thus different properties
structural isomers
cis-trans
enantiomers
structural isomers
same molecular formula, but covalent arrangement of carbon skeletons are different between isomers
may also differ in location of double bonds
the more carbons, the more possible isomers
cis-trans isomers
carbons are covalently bonded to same atoms but those atoms have different spatial arrangements due to inflexibility of double bonds (cannot rotate around bond axis without changing compound)
cis: atoms on same side of double bond
trans: atoms on opposite sides of double bond
this subtle difference can have huge effect on biological activities of organic molecules
enantiomers
isomers that are mirror images of each other and differ in shape because of asymmetric carbon (carbon covalently bonded to 4 different atoms)
left-and-right-handed versions of molecule
functional groups + list
chemical groups directly involved in chemical reactions; each has certain properties that dictates the way they behave in chemical reaction, is associated with carbons
hydroxyl, carboxyl, amino, sulfhydryl, phosphate, methyl groups
adenosine triphosphate (ATP)
organic phosphate
adenosine (organic molecule) attached to three phosphate groups
stores the potential to react with water/other molecules
Carbon chains vary in 4 ways
length
double bond position
branching
presence of rings
Distinctive properties of organic molecules depend on
the carbon skeleton and chemical groups attached to it