front 1 Explain how carbon's electron configuration explains its ability to form large,complex and diverse organic molecules | back 1 it has four valence electrons which can form many covalent bonds, of different combinations of single and double bonds,and multiple carbon atoms can form long chains such as gasoline. |
front 2 Describe 4 ways carbon skeletons may vary, and explain how this
variation | back 2 Covalent bonds link carbon atoms together in long chains that form
the skeletal framework for organic molecules. These carbon skeletons
may vary in: |
front 3 Name the 6 major functional groups found in organic molecules. ACCHPS | back 3 Amino, Carbonyl, Carboxyl, Hydroxyl, Phosphate, Sulfhydryl |
front 4 Amino functional group | back 4 Consists of nitrogen atom bonded to two hydrogens (-NH2) |
front 5 Carboxyl functional group | back 5 acidic, tends to drop a proton, forms with amines to make amino acids Amino acids are linked together by covalent bonds that are formed between amino and carboxyl containing groups Consists of a carbon double-bonded to an oxygen and also attached to a hydroxyl group (-COOH) |
front 6 Carbonyl functional group | back 6 acts as an acid, tends to lose a proton in solution. found on aldehyde and ketone molecules. The carbonyl functional group is the site of reactions that link these molecules into more complex compounds like ribose Consists of a carbon double-bonded to an oxygen (CO) |
front 7 Hydroxyl functional group | back 7 Hydroxyl groups act as weak acids. Highly polar, molecules with hydroxyl groups are soluble. Defining functional group of alcohols such as ethanol and methanol |
front 8 Phosphate functional group | back 8 Phosphate groups carry two negative charges and they go from one
molecule to another, the two negative charges often greatly affects
the receiving molecule |
front 9 Sulfhydryl functional group | back 9 Sulfhydryl groups are a sulfur atom bonded to a hydron atom, they link up with disulfides S-S bonds. In proteins, they form disulfide bonds that contribute to protein structure |
front 10 Describe the basic structure of a hydrocarbon and explain why these molecules are hydrophobic. | back 10 Hydrocarbons consists of only carbon and hydrogen. The nonpolar C-H bonds in hydrocarbon chains account for their hydrophobic properties |
front 11 Distinguish among the three types of isomers: structural, geometric, and enantiomer. | back 11 Structural isomers differ in the covalent arrangement of atoms and
often in the location of double bonds. |
front 12 Name the major chemical groups found in organic molecules. Describe the basic structure of each chemical group and outline the chemical properties of the organic molecules in which they occur. | back 12 Hydroxyl group consists of an oxygen and hydrogen (-OH). Carbonyl
group consists of a carbon double-bonded to an oxygen (CO).
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front 13 Explain how ATP function as the primary energy transfer molecules in living cells | back 13 One phosphate molecule, adenosine triphosphate (ATP), is the primary
energy-transferring molecule in the cell |