Term
|
Definition
|
|
Term
|
Definition
| Organic molecules consisting only of Carbon and Hydrogen. |
|
|
Term
|
Definition
| Structural, Geometric, and Enantiomers |
|
|
Term
|
Definition
| Differ in the covalent arrangements of their atoms. Number increases as carbon skeleton length increases. May differ in location of double bonds. |
|
|
Term
|
Definition
| Same covalent partnerships but differ in their spatial arrangement. Arrise from infelxability of double bonds. Differences can drastically alter their biological function. |
|
|
Term
|
Definition
| Mirror images. Differences important in pharmaceutical industry, Example of L-Dopa. |
|
|
Term
|
Definition
| Components of organic molecules most commonly involved in chemical reactions. Replace a H on a C chain. Each one behaves ina characteristic manner. |
|
|
Term
| Structure of a Hydroxyl Group |
|
Definition
|
|
Term
| Name of compunds with a Hydroxyl Group |
|
Definition
| Alcohols, names end in 'ol |
|
|
Term
| Example of a compound with a Hydroxyl Group |
|
Definition
|
|
Term
| Properties of the Hydroxyl Group |
|
Definition
Is Polar because of the electronegativity of the O atom pulling electrons towards it. Attracts water molecules, helps to dissolve organic compounds like sugars. |
|
|
Term
| Structure of a Carbonyl Group |
|
Definition
|
|
Term
| Name of compunds with a Carbonyl Group |
|
Definition
Ketones if the Carbonyl Group is within the C chain Aldehyde if the Carbonyl Group is at the end of a C chain. |
|
|
Term
| Example of compunds with Carbonyl Group |
|
Definition
Acetone, the simplest ketone, C3H6O1 Propanol, an Aldehyde, C3H6O1 |
|
|
Term
| Propeties of Carbonyl Group |
|
Definition
| A Ketone and an Aldehyde may be structural isomers with different properties like Acetone and Propanol. |
|
|
Term
| Structure of Carboxyl Group |
|
Definition
|
|
Term
| Name of compunds with a Carboxyl Group |
|
Definition
| Carboxylic Acids, or Organic Acids |
|
|
Term
| Example of compund with a Carboxyl Group |
|
Definition
|
|
Term
| Properties of compunds with Carboxyl Group |
|
Definition
| Has a source of H+ ions so they are acidic. These H+ ions dissociate reversibly due to the polarity of H bonded to O. In cells found as the Carboxylate Group as the ionic form. |
|
|
Term
| Structure of the Amino Group |
|
Definition
|
|
Term
| Name of Compunds with Amino Group |
|
Definition
|
|
Term
| Example of Compound with Amino Group |
|
Definition
Glycine, C2H5O2N Actually, Glycine is both an Amine and a Carboxylic Acid. |
|
|
Term
| Functional Properties of Amine Groups |
|
Definition
Acts as a base, can pick up H+ Ionized with a 1+ charge in cellular conditions |
|
|
Term
| Structure of a Sulphydryl Group |
|
Definition
|
|
Term
| Names of Compunds with a Sulphydryl Group |
|
Definition
|
|
Term
| Example of a compound with a Sulphydryl Group |
|
Definition
|
|
Term
| Properties of compounds with Sulphydryl Group |
|
Definition
| Two Sulphydryl Groups can interact to help stabilize protein structure |
|
|
Term
| Structure of a Phosphate Group |
|
Definition
|
|
Term
| Name of compounds with a Phosphate Group |
|
Definition
|
|
Term
| Examples of a compound with a Phosphate Group |
|
Definition
| C3H7O6P Glycerol Phosphate |
|
|
Term
| Functional properties of compounds with Phosphate Groups |
|
Definition
Makes the molecule of which it is a part a anion Can transfer energy between organic molecules |
|
|
Term
|
Definition
| Adenosine Triphosphate, the primary energy transfer molecule in the cell. |
|
|