Flashcards on Chapter 12
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unsaturated compounds contain places where |
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more hydrogen can be added |
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halogen substituents get treated the same as |
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alkyl groups |
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unsaturated means |
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that you can add hydrogen |
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compounds with double bonds suffix |
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-ene |
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suffix for compounds with triple bonds |
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-ynes |
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alkenes...cis or trans isomers possible |
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no |
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alkenes: noncyclic isomers possible? |
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no (no linear isomers possible) |
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When naming alkenes, name the longest continual chain the contains the |
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double bond (functional group) |
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number the chain so that the double bond has the |
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lowest possible number |
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more than one double bond called |
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-diene, -triene, etc |
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the central carbons in a double bond have a bond angle of |
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120 degrees |
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and the geometry of a double bond is |
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triagonal planar |
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the carbons in the alkene are |
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hybridized sp2 |
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the sp2 hybridized carbons form (blank) bonds |
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single |
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what forms the double bond? |
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remaining p orbital |
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sigma bonds are |
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single bonds |
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pi bonds |
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second bond of the double bond |
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is the double bond rigid |
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yes |
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is rotation possible around a double bond? |
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no |
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because double bonds are possible |
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cis/trans isomers (stereoisomers) |
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do all alkenes have stereoisomers? |
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no |
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which hydrogens do you look at when deciding if its cis or trans? |
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the hydrogens on the double bond |
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are alkenes polar |
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no (nonpolar) |
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are alkenes soluble in water? |
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no |
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are alkenes soluble in non-polar solvents? |
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yes |
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molecules with four or less carbons are what state? |
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state |
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molecules with four to seventeen carbons are what state |
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liquid |
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more than 17 carbons what state? |
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solid |
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are alkenes more or less dense than water? |
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less dense |
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type of intermolecular forces effect what physical properties? |
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melting point and boiling point |
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is the connectivity the same in geometric isomers? |
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yes |
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alkenes undergo what kind of reactions? |
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addition |
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addition reactions |
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two compounds are added together to form one new compound |
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in addition reactions, what happens to the double bond? |
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it disappears |
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addition of hydrogen is called |
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hydrogenation |
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the product of halogenation is a |
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haloalkane (alkyl halide) |
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When naming halides have the same priority as (blank) groups |
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alkyl |
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what is used in the lab to test for functional groups? |
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bromine |
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in the lab, what happens to a solution that has an alkene or alkyne present when bromine is added? |
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the bromine quickly disappears |
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hydrohaligenation |
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reactions with hydrogen halides |
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hydrohalogenation works well with |
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HCl, HF, HBr, HI |
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in hydrohalogenation the hydrogen adds to the carbon which... |
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already has the most hydrogens (markovnikovs rule) |
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hydration must have what present? |
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sulfuric acid as a catalyst |
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what type of reaction is hydration? |
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equilibrium |
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polymer |
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very large molecule jmade up of repeating units |
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monomers |
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starting materials |
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copolymer |
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addition product made of two or more monomers |
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Polymers shave how many dimensions? |
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two or three |
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addition polymeration |
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addition reaction between double bonded compounds |
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reaction mechanisms |
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the steps responsible for a reaction |
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the reaction mechanism for hydration is similar to |
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hydrohalogenation |
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hydration reaction step one |
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addtion of hydrogen |
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hydration step 2 |
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water adds to the carbocation |
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hydration step 3 |
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a hydrogen ion regenerated |
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alkynes |
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compounds with triple bonds |
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ethyne common name |
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acetylene |
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alkynes are the named the same way as |
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alkenes |
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are cis/trans possible for alkynes |
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no |
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alkynes have a (blank) hybridization |
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sp |
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aromatics are much less reactive than other compounds that contain |
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double or triple bonds |
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what kind of reactions do aromatics undergo when they do react? |
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substitution reactions |
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polycyclic aromatic compounds are often |
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carcinogenic |
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why are polycyclic aromatic compounds carcinogens? |
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they intercalate into dna and cause mutations |