First exam Flashcards
Oils are lipids. Which statement best explains why oil and water don’t mix?
Responses
If you try to mix oil and water, the two will separate almost immediately.
Oils and waxes are frequently used as water repellents—often as a coating on the surface of furniture or automobiles.
The C-C and C-H bonds that dominate oil molecules interact with each other—not water.
The C-C and C-H bonds that dominate oil molecules interact with each other—not water.
Explain how saturation relates to hydrophobic interactions
Lipids:
Saturated hydrocarbon chains pack together more tightly than unsaturated chains, so are held together more tightly by hydrophobic interactions.
Lipids vary a great deal in fluidity. Waxes, for example, are solid at room temperature while oils are liquid. Predict which of the following attributes are typical of the hydrocarbon chains in waxes versus more-fluid lipids. Select all that apply.
Responses
The hydrocarbon chains of waxes are saturated; those found in oils are not.
The hydrocarbon chains of waxes are polyunsaturated—meaning that they contain more than one double bond.
The hydrocarbon chains of waxes are longer than the chains found in oils.
Unlike oils, the hydrocarbon chains of waxes contain atoms other than C and H.
The hydrocarbon chains of waxes are saturated; those found in oils are not.
The hydrocarbon chains of waxes are longer than the chains found in oils.
Unlike oils, the hydrocarbon chains of waxes contain atoms other than C and H.
Fats contain highly electronegative oxygen atoms, which carry a partial charge. Which of the following is the most logical explanation for why fats are not soluble in water?
Responses
Numbers and geometry: C-O and O-H bonds are very few in number compared with nonpolar bonds, and the few O atoms are “buried” by hydrophobic groups.
The oxygen atoms in fats are less electronegative than the oxygen atoms in water, so carry less of a partial charge.
If fats were soluble in water, they could not perform their various functions in organisms, starting with energy storage and metabolism.
Numbers and geometry: C-O and O-H bonds are very few in number compared with nonpolar bonds, and the few O atoms are “buried” by hydrophobic groups.
Each fatty acid found in a fat consists of a long hydrocarbon chain that ends in a carboxl group (COOH, or O=C-OH). Why is “fatty acid” an appropriate name?
Responses
Fats vary in structure because they can contain more than one type of fatty acid, and because fatty acids vary in the length and saturation of their hydrocarbon chains.
“Fatty” refers to the long hydrocarbon chain; the carboxyl group acts as an acid by dropping a proton, just like the carboxyl groups in amino acids.
Carbon can form a total of four covalent bonds, so the C in the carboxyl group of a fatty acid can form a C-C bond with the hydrocarbon chain.
“Fatty” refers to the long hydrocarbon chain; the carboxyl group acts as an acid by dropping a proton, just like the carboxyl groups in amino acids.
Why is “phospholipid” an appropriate name?
Responses
These molecules contain a phosphate group (“phospho”) and a hydrocarbon tail that does not interact with water (“lipid”).
The two hydrocarbon chains that make up the tail can be long or short and saturated or unsaturated.
The head region has a polar group that adds to the strongly hydrophilic nature of the phosphate group.
These molecules contain a phosphate group (“phospho”) and a hydrocarbon tail that does not interact with water (“lipid”).
Cholesterol is an example of what class?
Steroids: type of lipid
The R-groups on the amino acids that make up either end of the molecule carry full charges or polar groups. But the R-groups that hang off the a-helix in the middle of this molecule are not polar or charged. Is this molecule amphipathic?
Responses
Yes, because the entire molecule is hydrophilic.
Yes, because some regions are polar and will interact with water while other regions are not polar and will not interact with water.
No, because more than one region is polar.
Yes, because the entire molecule is hydrophobic.
Yes, because some regions are polar and will interact with water while other regions are not polar and will not interact with water.
How do amphipathic lipids behave in water?
vesicle formation:
The hydrophobic tails of the phospholipids interact with each other, while the hydrophilic heads interact with water molecules inside and outside the vesicle.
Which of the following is the best characterization for a process that is spontaneous?
It is energetically favorable and results in products that are more stable.
What does it mean to say that vesicle formation is spontaneous?
phospholipids “naturally” form vesicles in water because they are more stable that way. The stability is based in
part on 1) hydrophobic interactions among the hydrocarbon tails on phospholipids in a bilayer
part 2) on hydrogen bonding between water molecules and the hydrophilic heads on phospholipids.
lipid:
Lipid: A molecule that does not dissolve in water.
Indicate which of the following statements about C, O, H, and N atoms are correct.
The number of covalent bonds each can form is hydrogen (1), oxygen (2), nitrogen (3), and carbon (4).
O is so electronegative that all of the covalent bonds it forms are polar — even the O=O double bonds in atmospheric oxygen (O2).
Their relative electronegativities are C = H < N «_space;O.
Nitrogen is found in nucleotides and nucleic acids but not in amino acids or proteins.
C-C and C-H bonds are nonpolar, so organic molecules that contain all or mostly all C and H atoms don’t contain partial charges, can’t participate in H-bonds, and tend not to dissolve in
The number of covalent bonds each can form is hydrogen (1), oxygen (2), nitrogen (3), and carbon (4).
Their relative electronegativities are C = H < N «_space;O.
C-C and C-H bonds are nonpolar, so organic molecules that contain all or mostly all C and H atoms don’t contain partial charges, can’t participate in H-bonds, and tend not to dissolve in
Difference between ribose and deoxyribose?
ribose: sugar in deoxyribonucleic acid (DNA)
deoxyribose: sugar in ribonucleic acid (RNA)
Suppose you are analyzing a glycan you have never seen before. Where would you find the glycosidic linkages?
Between each of the monosaccharide subunits in the long chain that forms the glycan.