Chemistry Chapter 13 Test Questions – Flashcards

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HO-
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hydroxyl group
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alcohols
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the -OH group is attached to the aliphatic portion of the compound
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phenols
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the -OH is attached to the aliphatic portion of a compound (not a benzene ring)
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ethers
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the oxygen is attached to two carbon atoms
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alcohols are classified into what categories?
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primary, secondary, tertiary
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alcohols with 1 to 12 carbons will be what state?
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liquid
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why do alcohols have higher bp?
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because of the hydrogen bonding of hydroxyl group
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one two and three carbon alcohols are
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miscible in water
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alcohols with more than five carbons will have minimal
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water solubility
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what has the greatest effect on boiling point?
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intermolucular forces
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alkanes soluble or insoluble in water
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insoluble
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for something to be soluble in water it must be able to form
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hydrogen bondswith water or at least accept them
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water solubility rule of thumb, one O, N or F allows solubility of
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3 to 4 carbons, attached to hydrogens
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if there are two or more -OH groups
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greater solubility, and higher bp
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more hydrogen bonds, greater or less solubility?
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greater
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the more hydrogen bonds the higher or lower the bp?
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higher
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the less carbons you have the higher or lower the bp?
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higher
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for reactions what four thing do you want to look at?
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the reagents, the functional groups, carbons with functional groups attached and adjacent carbon atoms
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dehydration
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the loss of a water molecule
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in dehydration the -OH and -H must be lost from
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adjacent carbon atoms
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the first product in a reaction
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predominates over the second (80/20)
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take the Hydrogen off the carbon with
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the least number of hydrogens to begin with
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type of reaction that forms ether
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condensation reaction
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oxidation
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the gain of bonds or loss of bonds to Hydrogen
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carbonyl group
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carbon must bond with hydrogen or carbon
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when oxidizing an organic compound
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a H must also be attached to the c atom undergoing oxidation
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oxidation of primary alcohols give
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carboxylic acid
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the oxidation of secondary alcohols gives
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ketones
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the oxidation of a tetiary compound yields
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no reaction
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alcohol plus sulfuric acid=
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dehydration
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alcohol plus oxygen=
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oxidation
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dehydration at a high temp gives
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alkenes
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dehydration at a low temp gives
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ether
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common alcohols
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methanol, ethanol, prpanol, ethylene glycol and glycerol
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methanol is used to make
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formaldehyde and MTBE
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ethanol is commonly called
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grain alcohol
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isopropyl is used for a solvent for
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medicines
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how many -OH groups does ethylene glycol have
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two
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is ethylene glycol soluble in water
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yes, miscible
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phenol is
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hydroxybenzene
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cholorseptic is
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one percent phenol
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which is more acidic alcohol or phenol?
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phenol
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the ion resulting from the loss of hydrogen from an alcohol
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alkoxide
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the ion resulting from the loss of hydrogen from phenol
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phenoxide ion
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alcohols are about as acidic as
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water
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ethers polar or nonpolar
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polar
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are small ethers soluble in water
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yes
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ehters can accept (blank) but cannot donate (blank)
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hydrogen bonds, hydrogen for hydrogen bonds
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heterocyclic compound
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something substituted in for carbon in a cyclic compound
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does the ether group take priority?
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no
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are ehter polar
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slightly
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is ether flammable
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yes
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is ether very reactive?
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no
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original anesthetic
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diethyl ether
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two natural ether products
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plant oils, and growth regualtors
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epoxicles
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three membered rings, very reactive
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bond angles of epoxides
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sixty degree
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thiols and disulfides contain
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sulfur
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thiols are sulfur analogs of
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alcohols
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also called
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mercaptans
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to name add (blank) to the parent hydrocarbon
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thiol
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what is crysteine?
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amino acids
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crysteine can form
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disulfide linkages
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disulfides formed by
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triols when in the presence of a mild oxidizing agent
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disulfides are biologically important for
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protein structure and stability
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heavy metals such as lead and mercury react with thiols to form
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insoluble compounds
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polyfunctional compounds
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biological molecules that have more than one functional groups
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