Understanding Curve Arrow Notation in Organic Chemistry

Understanding Curve Arrow Notation in Organic Chemistry

Assessment

Interactive Video

Chemistry

10th Grade - University

Hard

Created by

Jackson Turner

FREE Resource

This video tutorial covers the use of curve arrow notation in organic chemistry, focusing on electron flow in reactions. It explains the difference between full and half arrows, and their application in acid-base and radical reactions. The video also discusses homolytic and heterolytic bond cleavage, emphasizing the role of electronegativity. Additionally, it covers nucleophilic substitution reactions and the drawing of resonance structures. The tutorial concludes with information on additional resources and study tips for organic chemistry students.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What does a full arrow represent in curve arrow notation?

The flow of two electrons

The flow of a proton

The flow of a neutron

The flow of one electron

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In a radical reaction, what type of arrow is used to show the movement of electrons?

Curved arrow

Straight arrow

Full arrow

Half arrow

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the result of a homolytic bond cleavage?

Formation of ions

Formation of radicals

Formation of a new bond

No change

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In heterolytic bond cleavage, which atom receives the electrons?

The more electronegative atom

The atom with a negative charge

The less electronegative atom

The atom with a positive charge

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is formed when a carbon-bromine bond undergoes heterolytic cleavage?

Carbanion and hydrogen ion

Carbocation and hydrogen ion

Carbanion and bromide ion

Carbocation and bromide ion

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In a nucleophilic substitution reaction, what role does hydroxide play?

Electrophile

Nucleophile

Radical

Base only

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What happens to the electrons in a carbon-bromine bond during a nucleophilic substitution reaction?

They move to the carbon atom

They are shared equally

They form a new bond

They move to the bromine atom

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