Back to marketplace

Finalsss

No description yet. This curated deck is ready for daily study.

Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

Refers to the class of organic compounds that contain benzene-like, six-membered rings with 3 double bonds.

Back (Answer)

AROMATIC

#2
Front (Question)

Benzene Molecular Formula

Back (Answer)

C6H6

#3
Front (Question)

Properties of Aromatic

Back (Answer)

Cyclic-Benzene-like, six-membered rings

#4
Front (Question)

electron poor, has a positive charge and electron lovers

Back (Answer)

ELECTROPHILE

#5
Front (Question)

electron rich, has a negative charge

Back (Answer)

NUCELOPHILE

#6
Front (Question)

Compounds containing halogen bonded to a saturated sp3-hybridized carbon atom

Back (Answer)

ALKYL HALIDES

#7
Front (Question)

Synthesis of alkyl halides from alcohols

Back (Answer)

Preparation of Alkyl Halides

#8
Front (Question)

Formation and protonation of Grignard reagents

Back (Answer)

Reactions of Alkyl halides

#9
Front (Question)

Alkyl halides react with Magnesium metal in ether solvent to yield organomagnesium halides.

Back (Answer)

Grignard Reagents

#10
Front (Question)

The entering nucleophile attacks the substrate from a direction 180º away from the leaving group, resulting in an umbrella-like inversion of configuration at the C atom.

Back (Answer)

Nucleophilic Substitution Reaction o SN2 reaction

#11
Front (Question)

 Base abstracts a proton at the same time that the leaving group departs.

Back (Answer)

Eliminations o E2 reaction

#12
Front (Question)

the substrates spontaneously dissociates to form a carbocation, which can subsequently lose H+ from a neighboring carbon

Back (Answer)

Eliminations o E1 reaction

#13
Front (Question)

: far higher than alkyl halide and alkanes with the same molecular wt.

Back (Answer)

BP of alcohols

#14
Front (Question)

far higher than other aromatic hydrocarbons o = Because of hydrogen bonding

Back (Answer)

BP of phenols:

#15
Front (Question)

Reduction of Aldehydes to Give

Back (Answer)

Primary Alcohol

#16
Front (Question)

Reduction of Ketones to Give

Back (Answer)

Secondary Alcohol

#17
Front (Question)

Reduction of Esters to Give

Back (Answer)

Primary Alcohol

#18
Front (Question)

Reduction of Carboxylic Acids to Give

Back (Answer)

Primary Alcohol

#19
Front (Question)

Dehydration to Give

Back (Answer)

Alkenes

#20
Front (Question)

Oxidation to Give

Back (Answer)

Carbonyl Compounds

#21
Front (Question)

Synthesis of Ethers

Back (Answer)

o Wiliamson Ether Synthesis o Epoxides

#22
Front (Question)

Reaction of ethers

Back (Answer)

o Acidic cleavage with HBr or HI o Epoxides cleavage with aqueous acids

#23
Front (Question)

Production of carbonyls

Back (Answer)

 Alcohols > Aldehydes > Carboxylic acids  Alcohols > Ketones

#24
Front (Question)

Common oxidizing reagent

Back (Answer)

• PCC • CrO3, Na2Cr2O7