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124 Cards in this Set
- Front
- Back
STERIC NUMBER
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(# OF ATOMS BONDED TO CENTER ATOM ) + (# LONE PAIRS ON CENTRAL ATOMS)
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LAW OF MULTIPLE PROPORTIONS
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COMPARISON BETWEEN 2 DIFFERENT COMPOUNDS
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LAW OF DEFINITE PROPORTIONS
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APPLIES TO A SINGLE COMPOUND (RATIO OF MASS IS CONSTANT)
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IONIC BONDING (3)
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*ELECTRONS LOST AND GAINED
*TRY TO BE LIKE NOBLE GASES *METAL + NON METAL ONLY (SALT) |
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COVALENT BONDING (6)
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*ELECTRONS SHARED
*CHEMICAL BOND *NOT IONIC B/C NOT SALT *NOT ACID B/C NO CHARGES *NO CHARGED PARTICLES B/C NO METALS *NO ELECTRICITY |
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POLAR COVALENT BOND
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UNEQUAL SHARING OF E-
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VALENCE SHELL ELECTRON PAIR REPULSION MODEL (VSEPR MODEL)
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IMPLIED SHAPE OF E- PAIRS
NOT MOLECULAR SHAPE LINEAR SHAPE - 2 ATOMS TRIANGULAR TETRAHEDRON NON LINEAR OF V SHAPED |
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LONE PAIRS
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NOT ATOMS
JUST 2E- THAT STILL NEED SPACE |
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DIPOLE
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MOLECULE HAS POS AND NEG SIDE
IS CONSIDERED POLAR TEND TO DISSOLVE IN OTHER DIPOLE SPECIES EX) OIL NOT DISSOLVE IN WATER |
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NOMENCLATURE OF SALTS
*note for transition metals |
*METAL CATION = ELEMENT NAME
*NON METAL ANION = ELEMENT NAME + IDE SUFFIX TRANSITION METALS DONT HAVE VALENCE E- SO USE NUMBER F/ VALENCE E- OF OTHER NON TRANSITIONAL ELMENT |
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GREEK NUMBER PREFIX
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1 NO PREFIX
2 DI 3 TRI 4 TETRA 5 PENTA 6 HEXA 8 OCTA 10 DECA |
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NOMENCLATURE OF COVALENTLY BONDED COMPOUNDS
NON METAL + (NONMETAL or METALLOID) |
LEAST X ELEMENT W/ ATOM # PREFIX
MOST X ELEMENT WITH IDE SUFFIX & # PREFIX |
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ELECTRONEGATIVITY (X) TRENDS
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X INCR (UP) AND -->
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H3O+
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HYDRONIUM
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NH4+
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AMMONIUM
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OH–
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HYDROXIDE
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O2 2–
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PEROXIDE
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O2 –1
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SUPEROXIDE
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CO3 2–
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CARBONATE
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H2CO3
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CARBONIC ACID
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HCO3–
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HYDROGEN CARBONATE
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NO3–
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NITRATE
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HNO3
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NITRIC ACID
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NO2 –1
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NITRITE
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HNO2
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NITROUS ACID
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PO4 3–
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PHOSPHATE
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H3PO4
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PHOSPHORIC ACID
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HPO4 2–
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HYDROGEN PHOSPHATE
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H2PO4 –1
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DIHYDROGEN PHOSPHATE
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SO4 2–
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SULFATE
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H2SO4
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SULFURIC ACID
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SO3 2–
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SULFITE
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H2SO3
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SULFUROUS ACID
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HSO4 –1
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HYDROGEN SULFATE
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HSO3 –1
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HYDROGEN SULFITE
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CN–
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CYANIDE
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MnO4 –1
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PERMANGANATE
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CrO4 2–
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CHROMATE
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SCN–
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thiocyanate
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TREND IN ACID NAMES
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*if oxy-anion name ends in -ate the acid ends in -ic
*if oxy-anion name ends in -ite the acid ends in -ous |
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SOLUBILITY FOR NITRATES
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*NITRATES ALL SOLUBLE
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SOLUBILITY FOR AMMONIUM
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ALL SOLUBLE
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SOLUBILITY FOR
CHLORIDES BROMIDES IODIDES |
All are soluble except their Ag+, Pb 2+ and Hg2 2+ salts.
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SOLUBILITY FOR
HYDROXIDES OXIDES |
All hydroxides and oxides: insoluble with exception of alkalai metals & Ca2+, Sr2+ and Ba2+.
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SOLUBILITY FOR SULFIDES
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All sulfides: insoluble with the exception of
alkalai & alkaline earth metals (Group I & II metals). |
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H2SO4
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SULFURIC ACID
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SO3 2–
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SULFITE
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H2SO3
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SULFUROUS ACID
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HSO4 –1
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HYDROGEN SULFATE
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HSO3 –1
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HYDROGEN SULFITE
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CN–
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CYANIDE
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MnO4 –1
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PERMANGANATE
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CrO4 2–
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CHROMATE
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SCN–
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thiocyanate
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TREND IN ACID NAMES
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*if oxy-anion name ends in -ate the acid ends in -ic
*if oxy-anion name ends in -ite the acid ends in -ous |
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SOLUBILITY FOR NITRATES
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*NITRATES ALL SOLUBLE
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SOLUBILITY FOR AMMONIUM
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ALL SOLUBLE
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SOLUBILITY FOR
CHLORIDES BROMIDES IODIDES |
All soluble EXCEPT their Ag+, Pb 2+ and Hg2 2+ salts.
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SOLUBILITY FOR
HYDROXIDES OXIDES |
All hydroxides and oxides: INSOLUTLBE with EXCEPTION of alkalai metals & Ca2+, Sr2+ and Ba2+.
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SOLUBILITY FOR SULFIDES
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All sulfides: INSOLUBLE with the EXCEPTION of
alkalai & alkaline earth metals (Group I & II metals). |
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SOLUBILITY FOR
PHOSPHATES CARBONATES |
ALL phosphate & carbonates: INSOLUBLE with EXCEPTION of alkalai metals and ammonium.
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SOLUBILITY FOR SULFATES
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All sulfates are soluble with the exception of Ca2+, Sr2+, Ba2+ & Pb2+.
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PROCESS OF BALANCING A CHEMICAL REACTION IS JUSTIFIED BY:
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LAW OF CONSERVATION OF MASS
*ASSURES EQUAL # ATOMS BOTH SIDES *EQUAL CHARGES LEFT AND RIGHT |
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LIMITING REAGENT
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*WILL BE USED UP FIRST
*DEFINES THEORETICAL YIELD *NOT CALCULATED BY MASS PROPORTIONS *CHANGE F/ GRAMS->MOL AND COMPARE TO MOLES FROM BALANCED EQN |
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PERCENT YIELD
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(ACTUAL YIELD)/(THEORETICAL YIELD) ALL X 100 %
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STOCHIOMETRY
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MASS RELATIONS APPLIED TO BALANCE CHEMICAL REACTIONS
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SOLUTION
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*HOMOGENEOUS MIXTURE OF 2OR MORE SUBSTANCES
*AKA ALLOYS (METAL + SOLID) *USU DISSOLVED IN WATER *AQUEOUS SOLUTION |
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SOLVENT
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*ALWAYS ASSUME ITS WATER
*MAJOR COMPONENT *DISSOLVING MEDIUM |
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SOLUTE
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*MINOR COMPONENT
*PLACED ON SOLVENT |
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SATURATION
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ACHIEVED WHEN LIMIT TO HOW MUCH SOLUTE CAN BE DISSOLVED IN WATER IS REACHED.
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UNSATURATION
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BEFORE LIMIT IS REACHED
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SATURATION TREND
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COMPOUNDS: SIMILAR -> MIXED IN ANY PROPORTIONS
ALSO TEMP DEPENDENT |
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MISCIBLE
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NO LIMIT TO SOLUBILITY
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SUPER SATURATION SOLUTION
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*UNSTABLE SOLUTION
*WHEN SOLUBILITY LIMIT OF SUBSTANCE HAS BEEN EXCEEDED |
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NaC2H3O2
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SODIUM ACETATE
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MOLARITY (M)
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[MOLES SOLUTE (DISSOLVED MATERIAL)] / [LITERS SOLUTION (VOLUME)]
HIGH MOLARITY = LOTS OF SOLUTE IN SOLUTION [ACETONE] = MOLARITY OF ACETONE |
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C12H22O11
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SUGAR
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TYPES OF REACTIONS (3)
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1.DISSOLUTION/PRECIPITATION
2.OXIDATION REDUCTION (REDOX) 3.ACID BASE |
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PRECIPITATION
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PARTICLES F/ SOLUTION FORM A SOLID
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DISSOLUTION
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*GOES F/ SOLID TO LIQUID
*FORMS A CONDUCTING SOLUTION |
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SPECTATOR ION
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NON PARTICIPANT IN PRECIP RXN
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ELECTROLYTE
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*SUBSTANCE DISSOLVED IN H20
*PRODUCED BY DISSOLUTIN RXN *FORMS SEPARATE CATIONS/ANIONS |
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DIFFERENCE B/W PRECIPITATION IN SALTS
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SOLUBILITY
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SOLUBLE SALT
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*WILL DISSOLVE IN AQUEOUS SOLUTION
*IF >1 GRAM DISSOLVE IN 1 LITER |
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ACID
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*"DISSOLVES" METALS (PREATOMIC)
*SOUR TASTE *DYE LITMUS = RED *HAS IONIC BOND (HAS CHARGES = NOT COVALENT) *ELEMENT Y MUST HAV >X THAN H *IF =ELECT X,NOT POLAR, NOT ACID *H+ DONOR *NOT ACID UNLES H IS PRESENT |
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BASE
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*H+ ACCEPTOR
*BITTER TASTE *TURN LITMUS BLUE *LONE PAIR OF E- MUST BE PRESENT |
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CONJUGATE BASE OF ACID
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FRAGMENT LEFT AFTER H+ IS ACCEPTED
*TO GET IT REMOVE H+ FROM ACID |
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CONJUGATE ACID OF BASE
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*SPECIE PRODUCED WHEN H+ IS ACCEPTED
*TO GET IT ADD H+ TO BASE |
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DISSOLUTIN REACTION OF SALT AND WATER
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ANIONS AND CATIONS BREAK APART (PHYSICAL PROCESS NO CHEM CHANGE)
FORMULA IS CHEM CHANGE B/C SOMETHING NEW HAS BEEN CREATED. |
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HC2H3O2
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VINEGAR
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TREND IN SALT/ELECTROLYTES
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ALL SALTS ARE STRONG ELECTROLYTES CUS THEY GO 100% INTO ION FORMATION AS IT DISSOLVES.
*FEW IONS LOW CONDUCTIVITY. |
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EXAMPLES OF WEAK ACIDS
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VITAMIN C, ASPIRIN, CITRIC ACID
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EX) OF STRONG ACIDS
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HCL, SULFURIC ACID , NITRIC ACID
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H2SO4
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SULFURIC ACID
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HNO3
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NITRIC ACID
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OXIDES OF ELEMENTS
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*THEY ARE ANHYDRIDES OF ACIDS AND BASES.
*ADDING MORE OXYGEN TO AN ELEMENT MAKES IT MORE ACIDIC OR BASIC. |
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METAL OXIDE
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*BASE ANHYDRIDES
*MORE METTALLIC = STRONGER BASE |
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METAL OXIDES
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*BASE ANHYDRIDES
*MORE METALLIC = STRONGER BASE |
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NON METALLIC OXIDES
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*ACID ANHYDRIDES
*MORE NONMETALLIC = STRONGER ACID |
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AMPHOTERIC SUBSTANCE
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FUNCTIONS AS ACID AND BASE
EX) WATER CAN FUNCTION AS BOTH IT IS ALSO NEUTRAL |
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HALOGEN-HYDROGEN COMPOUNDS
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SPECIAL CLASS OF NON OXYGEN CONTAINING ACIDS
EX)HF, HCL, HBr, HI |
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H2CO3
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CARBONIC ACID
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NEUTRALIZATION REACTION
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WHEN A STRONG ACID REACTS WITH A STRONG BASE
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REDOX RXN FOR GRP 1 METALS
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+1
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REDOX RXN FOR GRP 2 METALS
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+2
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REDOX RXN FOR FLUORINE
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-1
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REDOX RXN FOR GRP 7
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-1 EXCEPT FOR COMPOUNDS WITH F OR O : FLUORINE OR OXYGEN WHERE IT CAN BE POSITIVE
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REDOX RXN FOR HYDROGEN
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+1 IN COMPOUNDS
-1 IN GRP 1 AND 2 METALS |
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REDOX RXN FOR OXYGEN
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-2 UNLESS W/ F (F TAKES PRECEDENCE)
-1 IN PEROXIDES LIKE H202 |
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REDUCTION
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*GAIN OF E-
*REDUCTION IN OXIDATION # |
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OXIDATION
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*LOSS OF E-
*INCREASE IN OXIDATIN # |
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REDUCIING AGENT
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*THE SUPPLIER/DONOR OF E-
*LOSING ELECTRONS *BEING OXIDIZED |
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OXIDIZING AGENT
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*THE ACCEPTOR OF E-
*GAINING ELECTRONS *BEING REDUCED |
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AVOGADRO'S LAW
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V IS PROP TO N (MOLES)
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CHARLES LAW
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V IS PROP TO T
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BOYLE'S LAW
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V IS INVERSLY PROP TO P
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IDEAL GAS LAW
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*PV=NRT
*PV = (G/MW)RT |
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DALTON'S LAW OF PARTIAL PRESSURE
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TOTAL PRESSURE = SUM OF INDIVIDUAL PRESSURES OF EACH GAS BY ITSELF
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PARTIAL PRESSURE
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PRESSURE EXERTED IF THE GAS WERE ALONE IN THE CONTAINER W/O OTHER GASES
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UNITS OF PRESSURE (3)
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*SI UNIT Pa
* 1 ATM = 101325 Pa = 760 mm Hg *TORR = mm Hg |
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UNITS OF VOLUME
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SI UNIT m3 BUT USU LITERS
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R: GAS LAW CONSTANT
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R = .08206 L ATM
_____________ MOL K |
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STP
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* STANDARD TEMP AND PRESSURE
* T = 273 K OR 0*C * P = 1 ATM |
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UNIT OF TEMP
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KELVIN
K = C + 273` |