Alkenes - IUPAC Names and Isomers

Alkenes - IUPAC Names and Isomers

Assessment

Interactive Video

Chemistry

10th - 12th Grade

Hard

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FREE Resource

The video tutorial covers the basics of alkenes, including their structure, bonding, and isomerism. It explains the IUPAC naming rules for alkenes, focusing on identifying the longest chain, numbering, and naming conventions. The tutorial also delves into the bonding characteristics of alkenes, highlighting the sigma and pi bonds, and the concept of SP2 hybridization. Additionally, it discusses the different types of isomerism in alkenes, such as structural and stereoisomerism, and the use of cis-trans and E-Z nomenclature.

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7 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the general formula for alkenes?

C_nH_2n

C_nH_2n+2

C_nH_n

C_nH_2n-2

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the IUPAC naming of alkenes, which group takes precedence when numbering the chain?

Halogens

Alkyl groups

Double bond

Hydroxyl groups

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What type of hybridization is present in the carbon atoms of alkenes?

sp

sp3d

sp2

sp3

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which type of bond is shorter in alkenes, sigma or pi?

Pi bond

Neither, it depends on the molecule

Sigma bond

Both are equal

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the main reason for restricted rotation around a double bond in alkenes?

Presence of a sigma bond

Presence of a pi bond

Presence of a single bond

Presence of a triple bond

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the term for isomers that differ in the spatial arrangement of groups around a double bond?

Geometrical isomers

Conformational isomers

Structural isomers

Optical isomers

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

According to the Cahn-Ingold-Prelog priority rules, what is an E isomer?

Low priority groups on opposite sides

Low priority groups on the same side

High priority groups on opposite sides

High priority groups on the same side