the chemistry of life unit:. chapter 2: the chemical context of life
TRANSCRIPT
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The Chemistry of
Life
Unit:
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Chapter 2:The Chemical Context of Life
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Matter consists of chemical elements in pure form and in combinations called compounds.
Matter is anything that takes up space and has mass.
An element is a substance that cannot be broken down to other substances by chemical reactions.
A compound is a substance consisting of two or more elements combined in a fixed ratio.
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C, H, O, N make up 96% of living matter. About 25 of 92 natural elements are known to be essential to life.
Trace elements are those required by an organism in only minute quantities (ex: iron, iodine)
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Element properties depend on the structure of its atoms.
(Theme???)
Each element consists of unique atoms
An atom is the smallest unit of matter that still retains the properties of an element
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Subatomic Particles
Atoms are composed of subatomic particles
Relevant subatomic particles include:Neutrons (no electrical charge)Protons (positive charge)Electrons (negative charge)
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• Atomic Nucleus: made up of neutrons and protons
• Electrons form a cloud around the nucleus
• Neutron mass and proton mass are almost identical and are measured in daltons
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Atomic Number and Atomic MassAtoms of the various elements differ in
number of subatomic particles Atomic number is the number of protons in
its nucleus An element’s mass number is the sum of
protons plus neutrons in the nucleus Atomic mass, the atom’s total mass,
can be approximated by the mass number
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Isotopes
All atoms of an element have the same number of protons but may differ in number of neutrons
Isotopes: two atoms of an element that differ in number of neutrons Ex: C-12 (~99%), C-13 (~1%), C-14 (<1%)
Radioactive isotopes: decay spontaneously, giving off particles and energy
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Some applications of radioactiveisotopes in biological research are:
• Dating fossils• Tracing atoms through metabolic processes• Diagnosing medical disorders
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The Energy Levels of Electrons
Energy: the capacity to cause change Potential energy: energy that matter has
because of its location or structure The electrons of an atom differ in their
amounts of potential energy An electron’s state of potential energy is
called its energy level, or electron shell
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Fig. 2-8
(a) A ball bouncing down a flight of stairs provides an analogy for energy levels of electrons
Third shell (highest energylevel)
Second shell (higherenergy level)
Energyabsorbed
First shell (lowest energylevel)
Atomicnucleus
(b)
Energylost
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Electron Distribution and Chemical Properties The periodic table of the elements shows the
electron distribution for each element
Valence electrons are those in the outermost shell, or valence shell The chemical behavior of an atom is mostly
determined by the valence electrons Elements with a full valence shell are chemically
inert
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The formation and function of molecules depend on chemical bonding between atoms
• Atoms with incomplete valence shells can share or transfer valence electrons with certain other atoms
• These interactions usually result in atoms staying close together, held by attractions called chemical bonds
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Covalent Bonds
Covalent bond: the sharing of a pair of valence electrons by two atoms In a covalent bond, the shared electrons
count as part of each atom’s valence shell
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A molecule consists of two or more atoms held together by covalent bonds
A single covalent bond, or single bond, is the sharing of one pair of valence electrons
A double covalent bond, or double bond, is the sharing of two pairs of valence electrons
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The notation used to represent atoms and bonding is called a structural formula
For example, H–H This can be abbreviated further with a molecular formula
For example, H2
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Polar/Nonpolar Covalent Bonds Nonpolar covalent bond: the atoms share the
electron equally Polar covalent bond: one atom is more
electronegative, and the atoms do not share the electron equally Unequal sharing of electrons causes a partial
positive or negative charge for each atom or molecule
Ex: H2O; oxygen is very electronegative and pulls
the shared electrons closer to its nucleus
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Ionic Bonds
Atoms sometimes strip electrons from their bonding partners
After the transfer of an electron, both atoms have charges
A charged atom (or molecule) is called an ion
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Na Cl Na Cl
NaSodium atom Chlorine atom
Cl Na+
Sodium ion(a cation)
Cl–Chloride ion
(an anion)
Sodium chloride (NaCl)
Fig. 2-14-2
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Animation: Ionic BondsAnimation: Ionic Bonds
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Cation: a positively charged ionAnion: a negatively charged ionIonic bond: an attraction between an
anion and a cation
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Hydrogen Bonds
Hydrogen bond: forms when a hydrogen atom covalently bonded to one electronegative atom is also attracted to another electronegative atom Ex: form between water molecules and
ammonia molecules In living cells, the electronegative partners
are usually oxygen or nitrogen atoms
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Van der Waals Interactions
If electrons are distributed asymmetrically in molecules or atoms, they can result in “hot spots” of positive or negative charge
Van der Waals interactions: attractions between molecules that are close together as a result of these charges Collectively, such interactions can be
strong, as between molecules of a gecko’s toe hairs and a wall surface
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Molecular shape and function
A molecule’s shape is usually very important to its function
A molecule’s shape is determined by the positions of its atoms’ valence orbitals
In a covalent bond, the s and p orbitals may hybridize, creating specific molecular shapes
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Fig. 2-17
s orbital Three porbitals
(a) Hybridization of orbitals
Tetrahedron
Four hybrid orbitals
Space-fillingModel
Ball-and-stickModel
Hybrid-orbital Model(with ball-and-stick
model superimposed)
Unbondedelectronpair
104.5º
Water (H2O)
Methane (CH4)
(b) Molecular-shape models
z
x
y
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Biological molecules recognize and interact with each other with a specificity based on molecular shape
Molecules with similar shapes can have similar biological effects
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Chapter 2 “Need to Knows”
The 3 types of subatomic particles and their significance.
The types of bonds, how they form, and their relative strengths.
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Overview: The Molecule That Supports All of Life
Overview: The Molecule That Supports All of Life
Water is the biological medium on EarthAll living organisms require water more
than any other substanceMost cells are surrounded by water, and
cells themselves are about 70–95% water
The abundance of water is the main reason the Earth is habitable
Water is the biological medium on EarthAll living organisms require water more
than any other substanceMost cells are surrounded by water, and
cells themselves are about 70–95% water
The abundance of water is the main reason the Earth is habitable
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The polarity of water molecules results in hydrogen bonding
The polarity of water molecules results in hydrogen bonding
• The water molecule is a polar molecule: The opposite ends have opposite charges
Polarity allows water molecules to form hydrogen bonds with each other
• The water molecule is a polar molecule: The opposite ends have opposite charges
Polarity allows water molecules to form hydrogen bonds with each other
Animation: Water StructureAnimation: Water Structure
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Fig. 3-2
Hydrogenbond
–H
+
H
O
——
——
+ +
+
–
–
–
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Four emergent properties of water contribute to Earth’s
fitness for life
Four emergent properties of water contribute to Earth’s
fitness for life• Four of water’s properties that
facilitate an environment for life are: Cohesive behavior Ability to moderate temperature Expansion upon freezing Versatility as a solvent
• Four of water’s properties that facilitate an environment for life are: Cohesive behavior Ability to moderate temperature Expansion upon freezing Versatility as a solvent
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CohesionCohesion
Collectively, hydrogen bonds hold water molecules together, a phenomenon called cohesion
Cohesion helps the transport of water against gravity in plants
Adhesion is an attraction between different substances, for example, between water and plant cell walls
Collectively, hydrogen bonds hold water molecules together, a phenomenon called cohesion
Cohesion helps the transport of water against gravity in plants
Adhesion is an attraction between different substances, for example, between water and plant cell walls
Animation: Water TransportAnimation: Water Transport
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Fig. 3-3
Water-conductingcells
Adhesion
Cohesion
150 µm
Directionof watermovement
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Surface tension is a measure of how hard it is to break the surface of a liquid
Surface tension is related to cohesion
Surface tension is a measure of how hard it is to break the surface of a liquid
Surface tension is related to cohesion
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Fig. 3-4
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Moderation of TemperatureModeration of Temperature
Water absorbs heat from warmer air and releases stored heat to cooler air
Water can absorb or release a large amount of heat with only a slight change in its own temperature
Water absorbs heat from warmer air and releases stored heat to cooler air
Water can absorb or release a large amount of heat with only a slight change in its own temperature
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Water’s High Specific HeatWater’s High Specific Heat
The specific heat of a substance is the amount of heat that must be absorbed or lost for 1 g of that substance to change its temperature by 1ºC
The specific heat of water is 1 cal/g/ºCWater resists changing its temperature
because of its high specific heat
The specific heat of a substance is the amount of heat that must be absorbed or lost for 1 g of that substance to change its temperature by 1ºC
The specific heat of water is 1 cal/g/ºCWater resists changing its temperature
because of its high specific heat
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Water’s high specific heat can be traced to hydrogen bondingHeat is absorbed when hydrogen bonds
breakHeat is released when hydrogen bonds
formThe high specific heat of water
minimizes temperature fluctuations to within limits that permit life
Water’s high specific heat can be traced to hydrogen bondingHeat is absorbed when hydrogen bonds
breakHeat is released when hydrogen bonds
formThe high specific heat of water
minimizes temperature fluctuations to within limits that permit life
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Evaporative CoolingEvaporative Cooling
Evaporation is transformation of a substance from liquid to gas
As a liquid evaporates, its remaining surface cools, a process called evaporative cooling
Evaporative cooling of water helps stabilize temperatures in organisms and bodies of water
Evaporation is transformation of a substance from liquid to gas
As a liquid evaporates, its remaining surface cools, a process called evaporative cooling
Evaporative cooling of water helps stabilize temperatures in organisms and bodies of water
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Insulation of Bodies of Water by Floating Ice
Insulation of Bodies of Water by Floating Ice
Ice floats in liquid water because hydrogen bonds in ice are more “ordered,” making ice less dense
This keeps large bodies of water from freezing solid and therefore moderate s temperature
Ice floats in liquid water because hydrogen bonds in ice are more “ordered,” making ice less dense
This keeps large bodies of water from freezing solid and therefore moderate s temperature
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Fig. 3-6a
Hydrogenbond
Liquid waterHydrogen bonds break and re-form
IceHydrogen bonds are stable
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The Solvent of LifeThe Solvent of Life
A solution is a liquid that is a homogeneous mixture of substances
A solvent is the dissolving agent of a solution
The solute is the substance that is dissolved
An aqueous solution is one in which water is the solvent
A solution is a liquid that is a homogeneous mixture of substances
A solvent is the dissolving agent of a solution
The solute is the substance that is dissolved
An aqueous solution is one in which water is the solvent
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Water is a versatile solvent due to its polarity, which allows it to form hydrogen bonds easily
When an ionic compound is dissolved in water, each ion is surrounded by a sphere of water molecules called a hydration shell
Water is a versatile solvent due to its polarity, which allows it to form hydrogen bonds easily
When an ionic compound is dissolved in water, each ion is surrounded by a sphere of water molecules called a hydration shell
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Fig. 3-7
Cl–
Na
Cl–
+
+
+
+
+
+
++
––
–
–
–
–
––
Na+
–
––
+
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Chapter 4:
CARBON AND THE MOLECULAR
DIVERSITY OF LIFE
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Carbon: The Backbone of Life
• Although cells are 70–95% water, the rest consists mostly of carbon-based compounds
• Carbon is unparalleled in its ability to form large, complex, and diverse molecules
• Proteins, DNA, carbohydrates, and other molecules that distinguish living matter are all composed of carbon compounds
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What properties of Carbon make it the molecular basis of life?
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Organic chemistry is the study of carbon compounds
• Organic chemistry is the study of compounds that contain carbon
• Organic compounds range from simple molecules to colossal ones
• Most organic compounds contain hydrogen atoms in addition to carbon atoms
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Carbon atoms can form diverse molecules by bonding to four
other atoms
• Electron configuration is the key to an atom’s characteristics
• Electron configuration determines the kinds and number of bonds an atom will form with other atoms
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The Formation of Bonds with Carbon
• With four valence electrons, carbon can form four covalent bonds with a variety of atoms
• This tetravalence makes large, complex molecules possible
• In molecules with multiple carbons, each carbon bonded to four other atoms has a tetrahedral shape
• However, when two carbon atoms are joined by a double bond, the molecule has a flat shapeCopyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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Fig. 4-3
NameMolecular Formula
Structural Formula
Ball-and-StickModel
Space-FillingModel
(a) Methane
(b) Ethane
(c) Ethene (ethylene)
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• The electron configuration of carbon gives it covalent compatibility with many different elements
• The valences of carbon and its most frequent partners (hydrogen, oxygen, and nitrogen) are the “building code” that governs the architecture of living molecules
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Fig. 4-4
Hydrogen(valence = 1)
Oxygen(valence = 2)
Nitrogen(valence = 3)
Carbon(valence = 4)
H O N C
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• Carbon atoms can partner with atoms other than hydrogen; for example:• Carbon dioxide: CO2
• Urea: CO(NH2)2
O = C = O
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Fig. 4-UN1
Urea
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Molecular Diversity Arising from Carbon Skeleton Variation
• Carbon chains form the skeletons of
most organic molecules
• Carbon chains vary in length and shape
Animation: Carbon SkeletonsAnimation: Carbon Skeletons
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Fig. 4-5: Variation in Carbon Skeletons
Ethane Propane1-Butene 2-Butene
(c) Double bonds
(d) RingsCyclohexane Benzene
Butane 2-Methylpropane(commonly called isobutane)
(b) Branching
(a) Length
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Fig. 4-5a
(a) Length
Ethane Propane
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Fig. 4-5b
(b) Branching
Butane 2-Methylpropane(commonly called isobutane)
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Fig. 4-5c
(c) Double bonds
1-Butene 2-Butene
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Fig. 4-5d
(d) RingsCyclohexane Benzene
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Hydrocarbons
• Hydrocarbons are organic molecules consisting of only carbon and hydrogen
• Many organic molecules, such as fats, have hydrocarbon components
• Hydrocarbons can undergo reactions that release a large amount of energy
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Fig. 4-6: The role of hydrocarbons in fats
( Black = carbon ) ( gray = hydrogen ) ( red = oxygen )
(a) Mammalian adipose cells (b) A fat molecule
Fat droplets (stained red)
100 µm
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Isomers
• Isomers are compounds with the same molecular formula but different structures and properties:• These differences can result in molecules that are
very different in their biological activities.
• Structural isomers have different covalent arrangements of their atoms
• Geometric isomers have the same covalent arrangements but differ in spatial arrangements
• Enantiomers (sterioisomers) are isomers that are mirror images of each other
Animation: IsomersAnimation: Isomers
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• Enantiomers are important in the pharmaceutical industry
• Two enantiomers of a drug may have different effects
• Differing effects of enantiomers demonstrate that organisms are sensitive to even subtle variations in molecules
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Fig. 4-8
Drug
Ibuprofen
Albuterol
Condition
Pain;inflammation
Asthma
EffectiveEnantiomer
S-Ibuprofen
R-Albuterol
R-Ibuprofen
S-Albuterol
IneffectiveEnantiomer
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A small number of chemical groups are key to the functioning
of biological molecules
• Distinctive properties of organic molecules depend not only on the carbon skeleton but also on the molecular components attached to it
• A number of characteristic groups are often attached to skeletons of organic molecules
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The Chemical Groups Most Important in the Processes of Life
• Functional groups are the components of organic molecules that are most commonly involved in chemical reactions
• The number and arrangement of functional groups give each molecule its unique properties
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• The seven functional groups that are most important in the chemistry of life:• Hydroxyl group• Carbonyl group• Carboxyl group• Amino group• Sulfhydryl group• Phosphate group• Methyl group
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Fig. 4-10aHydroxylCHEMICAL
GROUP
STRUCTURE
NAME OF COMPOUND
EXAMPLE
FUNCTIONALPROPERTIES
Carbonyl Carboxyl
(may be written HO—)
In a hydroxyl group (—OH), ahydrogen atom is bonded to anoxygen atom, which in turn isbonded to the carbon skeleton ofthe organic molecule. (Do notconfuse this functional groupwith the hydroxide ion, OH–.)
When an oxygen atom isdouble-bonded to a carbonatom that is also bonded toan —OH group, the entireassembly of atoms is calleda carboxyl group (—COOH).
Carboxylic acids, or organicacids
Ketones if the carbonyl group iswithin a carbon skeleton
Aldehydes if the carbonyl groupis at the end of the carbonskeleton
Alcohols (their specific namesusually end in -ol)
Ethanol, the alcohol present inalcoholic beverages
Acetone, the simplest ketone Acetic acid, which gives vinegarits sour taste
Propanal, an aldehyde
Has acidic propertiesbecause the covalent bondbetween oxygen and hydrogenis so polar; for example,
Found in cells in the ionizedform with a charge of 1– andcalled a carboxylate ion (here,specifically, the acetate ion).
Acetic acid Acetate ion
A ketone and an aldehyde maybe structural isomers withdifferent properties, as is thecase for acetone and propanal.
These two groups are alsofound in sugars, giving rise totwo major groups of sugars:aldoses (containing analdehyde) and ketoses(containing a ketone).
Is polar as a result of theelectrons spending more timenear the electronegative oxygen atom.
Can form hydrogen bonds withwater molecules, helpingdissolve organic compoundssuch as sugars.
The carbonyl group ( CO)consists of a carbon atomjoined to an oxygen atom by adouble bond.
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Fig. 4-10bCHEMICALGROUP
STRUCTURE
NAME OFCOMPOUND
EXAMPLE
FUNCTIONALPROPERTIES
Amino Sulfhydryl Phosphate Methyl
A methyl group consists of acarbon bonded to threehydrogen atoms. The methylgroup may be attached to acarbon or to a different atom.
In a phosphate group, aphosphorus atom is bonded tofour oxygen atoms; one oxygenis bonded to the carbon skeleton;two oxygens carry negativecharges. The phosphate group(—OPO3
2–, abbreviated ) is anionized form of a phosphoric acidgroup (—OPO3H2; note the twohydrogens).
P
The sulfhydryl groupconsists of a sulfur atombonded to an atom ofhydrogen; resembles ahydroxyl group in shape.
(may bewritten HS—)
The amino group(—NH2) consists of anitrogen atom bondedto two hydrogen atomsand to the carbon skeleton.
Amines Thiols Organic phosphates Methylated compounds
5-Methyl cytidine
5-Methyl cytidine is acomponent of DNA that hasbeen modified by addition ofthe methyl group.
In addition to taking part inmany important chemicalreactions in cells, glycerolphosphate provides thebackbone for phospholipids,the most prevalent molecules incell membranes.
Glycerol phosphate
Cysteine
Cysteine is an importantsulfur-containing aminoacid.
Glycine
Because it also has acarboxyl group, glycineis both an amine anda carboxylic acid;compounds with bothgroups are called amino acids.
Addition of a methyl groupto DNA, or to moleculesbound to DNA, affectsexpression of genes.
Arrangement of methylgroups in male and femalesex hormones affectstheir shape and function.
Contributes negative chargeto the molecule of which it isa part (2– when at the end ofa molecule; 1– when locatedinternally in a chain ofphosphates).
Has the potential to reactwith water, releasing energy.
Two sulfhydryl groupscan react, forming acovalent bond. This“cross-linking” helpsstabilize proteinstructure.
Cross-linking ofcysteines in hairproteins maintains thecurliness or straightnessof hair. Straight hair canbe “permanently” curledby shaping it aroundcurlers, then breakingand re-forming thecross-linking bonds.
Acts as a base; canpick up an H+ fromthe surroundingsolution (water, in living organisms).
Ionized, with acharge of 1+, undercellular conditions.
(nonionized) (ionized)
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Fig. 4-10c
STRUCTURE
EXAMPLE
NAME OFCOMPOUND
FUNCTIONALPROPERTIES
Carboxyl
Acetic acid, which gives vinegar its sour taste
Carboxylic acids, or organic acids
Has acidic propertiesbecause the covalent bond between oxygen and hydrogen is so polar; for example,
Found in cells in the ionized form with a charge of 1– and called a carboxylate ion (here, specifically, the acetate ion).
Acetic acid Acetate ion
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Fig. 4-10d
STRUCTURE
EXAMPLE
NAME OFCOMPOUND
FUNCTIONALPROPERTIES
Amino
Because it also has a carboxyl group, glycine is both an amine anda carboxylic acid; compounds with both groups are called amino acids.
Amines
Acts as a base; can pick up an H+ from the surrounding solution (water, in living organisms).
Ionized, with a charge of 1+, under cellular conditions.
(ionized)(nonionized)
Glycine
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Fig. 4-10e
STRUCTURE
EXAMPLE
NAME OFCOMPOUND
FUNCTIONALPROPERTIES
Sulfhydryl
(may be written HS—)
Cysteine
Cysteine is an important sulfur-containing amino acid.
Thiols
Two sulfhydryl groups can react, forming a covalent bond. This “cross-linking” helps stabilize protein structure.
Cross-linking ofcysteines in hairproteins maintains the curliness or straightness of hair. Straight hair can be “permanently” curled by shaping it around curlers, then breakingand re-forming thecross-linking bonds.
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Fig. 4-10f
STRUCTURE
EXAMPLE
NAME OFCOMPOUND
FUNCTIONALPROPERTIES
Phosphate
In addition to taking part in many important chemical reactions in cells, glycerol phosphate provides the backbone for phospholipids, the most prevalent molecules in cell membranes.
Glycerol phosphate
Organic phosphates
Contributes negative charge to the molecule of which it is a part (2– when at the end of a molecule; 1– when located internally in a chain of phosphates).
Has the potential to react with water, releasing energy.
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Fig. 4-10g
STRUCTURE
EXAMPLE
NAME OFCOMPOUND
FUNCTIONALPROPERTIES
Methyl
5-Methyl cytidine is a component of DNA that has been modified by addition of the methyl group.
5-Methyl cytidine
Methylated compounds
Addition of a methyl group to DNA, or to molecules bound to DNA, affects expression of genes.
Arrangement of methyl groups in male and female sex hormones affectstheir shape and function.
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ATP: An Important Source of Energy for Cellular Processes
• One phosphate molecule, adenosine triphosphate (ATP), is the primary energy-transferring molecule in the cell
• ATP consists of an organic molecule called adenosine attached to a string of three phosphate groups
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Review: The Chemical Elements of Life
• The versatility of carbon makes possible the great diversity of organic molecules
• Variation at the molecular level lies at the foundation of all biological diversity
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Fig. 4-UN5
P P P P i P PAdenosine Adenosine
ADPATP Inorganic phosphate
Reacts with H2O
Energy
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Chapter 4 “Need to Knows”
1. Explain how carbon’s electron configuration explains
its ability to form large, complex, diverse organic
molecules
2. Describe how carbon skeletons may vary and explain
how this variation contributes to the diversity and
complexity of organic molecules
3. Distinguish among the three types of isomers:
structural, geometric, and enantiomer
continued….
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4. Name the major functional groups found in organic molecules; describe the basic structure of each functional group and outline the chemical properties of the organic molecules in which they occur
5. Explain how ATP functions as the primary energy transfer molecule in living cells
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