Nomenclature - Crash Course Chemistry

Nomenclature - Crash Course Chemistry

Assessment

Interactive Video

Chemistry, Science

11th Grade - University

Hard

Created by

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The video explains the role of IUPAC in standardizing chemical nomenclature, emphasizing the importance of systematic naming for clarity and communication in chemistry. It outlines the steps for naming chemical compounds, including identifying the carbon chain length, functional groups, and their respective suffixes. The video also provides practical examples to illustrate the naming process, highlighting the benefits of a universal naming system.

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7 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary reason IUPAC changes familiar chemical names to systematic ones?

To make chemistry more challenging

To ensure universal understanding and minimize misinterpretation

To replace all traditional names with new ones

To create more complex names for fun

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

When naming a compound, what is the first step according to IUPAC rules?

Choosing a name that sounds appealing

Determining the number of hydrogen atoms

Finding the longest carbon chain

Identifying the functional groups

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What suffix is added to the name of a compound with a ketone functional group?

AMINE

ONE

OL

AL

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does IUPAC determine which functional group is the parent in a compound with multiple groups?

By the alphabetical order of the groups

By the size of the group

By a precedence list created by IUPAC

By the color of the compound

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the correct IUPAC name for a compound with a three-carbon chain and an aldehyde group?

Propane

Propyne

Propanal

Propene

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the example of angelic acid, what is the correct IUPAC name after considering the functional groups and numbering?

3-methylbut-2-en-4-oic acid

2-methylbut-2-enoic acid

Methylbutanoic acid

Butanoic acid

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is it important to use systematic names like Trans-3-phenylprop-2-enal instead of common names like Cinnamaldehyde?

To replace all historical names

To confuse non-chemists

To allow chemists to deduce the structure from the name

To make the names longer