ORGANIC
Master Your Organic Chemistry: The Electrophilic Challenge
Test your knowledge of organic chemistry with our engaging quiz, designed to challenge both students and enthusiasts alike. Dive deep into the world of electrophiles, alkenes, and carbocations!
- 12 thought-provoking questions
- Multiple-choice format
- Immediate feedback on your answers
Whats an electrophile?
A negatively charged element that can attack an alkyne
A positively charged element that can attack an alkene
A neutral element capable of liberating a proton
An element that induce an nucleophilic reaction
The general formula of an alkene is
CnH2n
CnH2n+2
CnH2n-2
CnH2n-1
If I have an alkene; In order to produce an alkane, I realize an
Electrophilic reaction
Hydrogenation
Halogenation
Hydratation
An alkene with the two lowest group on the same side has a
Cis position
Trans position
What is the most stable carbocation?
Tertiary
Primary
Secondary
Methyl
How many cyclic chain do we have?
1
2
3
4
5
What is a 1,2-shift?
Changing the protons number in an alkene
Changing the position of the carbons
Changing the conformation of an alkene into a cyclic chain
Changing carbon positions in order to create a more stable carbocation.
According to Markovnikov, the electrophile attach to
The most alkylated carbon
The most hydrogenated carbon
The most stable carbon
To the weakest carbocation
On which carbon will attach the Br?
C
CH2
CH3
In the presence of peroxide, we obtain:
1,2-shift
Markovnikov Reaction
Anti-Markovnikov
Ring expansion
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