Reactions of Alkenes and Haloalkanes

0.0(0)
studied byStudied by 0 people
call kaiCall Kai
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
GameKnowt Play
full-widthPodcast
1
Card Sorting

1/20

flashcard set

Earn XP

Description and Tags

Flashcards covering key reactions and properties of alkenes and haloalkanes.

Last updated 11:09 PM on 10/30/25
Name
Mastery
Learn
Test
Matching
Spaced
Call with Kai

No analytics yet

Send a link to your students to track their progress

21 Terms

1
New cards

Dihydroxylation

A reaction where osmium tetroxide adds to alkenes to introduce two -OH groups.

2
New cards

OsO4

Osmium tetroxide, a reagent used in the dihydroxylation of alkenes.

3
New cards

1,2-diol

A diol where two hydroxyl (-OH) groups are added to the first and second carbons.

4
New cards

Glycol

Another name for a 1,2-diol.

5
New cards

N-methylmorpholine N-oxide (NMO)

An oxidizing agent used in Upjohn dihydroxylation.

6
New cards

Ozonolysis

A reaction that uses ozone to cleave a C=C double bond, producing carbonyl compounds.

7
New cards

Molozonide

An intermediate formed in the ozonolysis reaction.

8
New cards

Ozonide

A compound formed when a molozonide rearranges.

9
New cards

Chain reaction

A reaction where the products initiate further reactions, typical of radical processes.

10
New cards

Initiation step

The first step in a chain reaction where radicals are formed.

11
New cards

Propagation step

The steps in a chain reaction that produce new radicals and continue the reaction.

12
New cards

Chain termination

The step in a chain reaction where radicals combine to form stable products.

13
New cards

Regioselectivity

Preference of a reaction to occur at one location over others in a molecular structure.

14
New cards

Stereochemistry of radical halogenation

The creation of a racemic mixture resulting from halogenation where a chiral center is formed.

15
New cards

Allylic radical

A radical formed on a carbon next to a C=C double bond, stabilized by resonance.

16
New cards

N-bromosuccinimide (NBS)

A reagent that can promote allylic bromination under radical conditions.

17
New cards

Non-Markovnikov addition

Addition of HX to an alkene in which the hydrogen adds to the least substituted carbon.

18
New cards

Autoxidation

A reaction that requires oxygen to oxidize an organic compound, usually initiated by a radical.

19
New cards

R-X

The general formula for haloalkanes, where R is an alkyl group and X is a halogen.

20
New cards

Chlorofluorocarbons (CFCs)

Compounds that were once used as refrigerants and propellants, harmful to the ozone layer.

21
New cards

PFASs (Per- and polyfluoroalkyl substances)

Organic compounds where hydrogen is replaced by fluorine, persistent in the environment.