acid/base, redox, and organic - chapter 4 - Chemistry of the environment

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40 Terms

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acid
a substance that, when dissolved in water, produces hydronium ions (H3O+)
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properties of acids

1. sour taste
2. turns blue litmus paper red
3. dissolve certain metals
4. undergoes reaction with bases
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base
* substance that, when dissolved in water, produces hydroxide ions (OH−)
* alkali
* caustic
* lye
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properties of bases

1. bitter taste
2. turns red litmus paper blue
3. slipperier soapy feel
4. undergoes reactions with acidspr
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products of neutralization reaction
* __**SALT**__
* water
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characteristics of the pH scale
* scale is inverse
* scale is nonlinear
* factors of ten
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solubility guidelines

1. The compounds of Na+, K+, and NH4+, and NO3-are all **water soluble**
2. Most compounds of Cl− are **water soluble**; ==exceptions== include ==AgCl==, and lead chloride, ==PbCl2==, which is only slightly soluble
3. Most **sulfates** are **water soluble**; ==exceptions== include ==PbSO4, Hg2SO4, Ag2SO4, and CaSO4==(slightly soluble)
4. Most **hydroxides** are **water insoluble**; ==exceptions== include ==NaOH, KOH, and Ca(OH)2== (slightly soluble)
5. Most **carbonates and phosphates** are **water insoluble**; ==exceptions== include ==compounds of Na+, K+, and NH4+==
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first definition of oxidation
The chemical combination of a substance with oxygen
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first definition of reduction
the chemical removal of second definition of oxygen from a substance
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second definition of oxidation
the chemical removal of second definitiohydrogen from a substance
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second definition of reduction
the chemical combination of a substance with hydrogen
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third definition of oxidation
loss of electrons from a chemical species
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third definition of reduction
gain of electrons by a chemical species
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organic chemistry
branch of chemistry dealing with the compounds of carbon
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structural formula
a drawing showing exactly which atoms are bonded to each other and the exact order of this bonding
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condensed structural formulas
grouping carbon and hydrogen atoms that are attached to each other
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line-bond formulas
many of the carbon atoms are shown as bends in a line (or in some cases as the end of a line), and many of the hydrogen atoms are omitted
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hydrocarbon
compound containing only carbon and hydrogen
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alk%%anes%%
* organic compounds containing only carbon, hydrogen, and %%single bonds%%
* %%saturated%% hydrocarbons
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first ten continuous-chain alkanes
knowt flashcard image
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isomers
compounds with the same molecular formula, but different structural formulas
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alk^^enes^^
* hydrocarbons that contain a carbon-to-carbon ^^double^^ bond
* general formula CnH2n
* ^^unsaturated^^ hydrocarbons
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ethylene
simplest alkene
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alk@@ynes@@
* hydrocarbons that contain a carbon-to-carbon @@triple@@ bond
* general formula CnH2n-2
* @@unsaturated@@ hydrocarbons
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ethyne (acetylene)
simplest alkyne
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benzene
unique organic compound with very stable six-sided ring
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aromatic hydrocarbons
contain a benzene ring or have properties similar to those of benzene
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functional groups
Atoms or groups of atoms attached to hydrocarbon skeletons that give the compounds characteristic chemical and physical properties
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alcohols
contain the hydroxyl (-OH) functional group
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phenols
* aromatic compounds with the hydroxyl group attached to the aromatic ring
* act as acids
* effective antiseptics
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ethers
* compounds with two alkyl groups bonded to the same oxygen
* general formula ROR
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carbonyls
C double bond O functional group
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aldehydes
carbonyl with hydrogen on one end and alkyl group on the other
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keynote
carbonyl with alkyl group on both ends
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carboxylic acids
organic acids with the carboxyl group (COOH)
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benzoic acids
carboxylic acid with benzene attached directly to the carboxyl group
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esters
derived from carboxylic acids and alcohols or phenols
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amines
derivatives of ammonia when one or more hydrogen of ammonia amidis replaced by an alkyl group
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amides
* nitrogen bonded to a carbonyl carbon
* amino acids of proteins are linked by amide linkages
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heterocyclic compounds
rings that contain atoms other than carbon as part of the ring