Exam 3 Flashcards

1
Q

Compounds containing both double and triple bonds are called

A

-enynes

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2
Q

When naming a compound that has both an alkene and alkyne, which one takes priority

A

Alkene

Ex)1-nonen-8-yne
1=Alkene on first carbon

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3
Q

What is the exception for an alkyne being a higher priority over Alkene

A

If a lower number can be assigned to the alkyne instead of the Alkene then the alkyne take priority

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4
Q

What is the exception if the Alkene and alkyne are equidistant

A

The whichever one is closest to the substituent is higher priority

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5
Q

CH3CH2CH2CH2

A

Butyl

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6
Q

1-Butenyl

A

CH3CH2CH=CH

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7
Q

1-Butynyl

A

CH3CH2C-=C
(Triple bond)

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8
Q

Vic in Al dihalides are prepared by

A

Addition of X2 to an Alkene

Add one H and a Hlogen to each carbon connected to the Alkene

Final product= alkane

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9
Q

How to prepare an alkyne (typically from alkane)

A

Strong base reagents: KOH or NaNH2

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10
Q

For halgenation: 1eq of X2 will produce

A

A trans Alkene

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11
Q

Halogenating reagents

A

Cl2 or Br2

CH3CO2H

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12
Q

Reagents for acid catalyzed Hydration

A
  1. HgSO4
  2. H2SO4, H2O

Produces. Ketone

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13
Q

Heats of hydrogenation shows

A

First step of this reaction is more exothermic than the second step

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14
Q

-176 kj/mol vs -137kj/Mol which is more exothermic

A

-176kj/mol

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15
Q

Describe connect break off method

A

A method for terminal alkynes to make a hydrocarbon
(Slide 1 of 9.2 slides)

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16
Q

Relationship between terminal alkynes and alkenes/alkanes

A

Terminal alkynes are more acidic than alkenes or alkanes

17
Q

Which base should I choose to create sodium acetylene: NaOH or NaNH2

Explain why

A

For deprotanation of an terminal alkyne we need the strongest base out of the two. NaNH2 is the strongest bc it has a stronger conjugate acid than NaOH

18
Q

SN1 step 1 reaction

A

Leaving group leaves and carbocation is formed

19
Q

For an inversion SN2 reaction what carbon changes it’s stereochemistry

A

The carbon bearing the leaving group is invented, meaning it changes stereochemistry

20
Q

For an SN2 reaction has a strong nucleophile it’s attacks from

A

The back and inversion of stereochemistry occurs