Stereochemistry - Crash Course Organic Chemistry

Stereochemistry - Crash Course Organic Chemistry

Assessment

Interactive Video

Created by

Quizizz Content

Chemistry, Science, Physics

11th Grade - University

Hard

The video explores the concept of chirality in organic chemistry, focusing on the significance of molecular structure and stereochemistry. It discusses isomers, particularly stereoisomers, and explains how chirality affects molecular behavior. The video introduces enantiomers, their naming conventions using the Cahn-Ingold-Prelog system, and the importance of spatial arrangement in determining molecular properties. It also covers chirality in cyclic compounds and how to identify achiral molecules.

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10 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What was the main reason Dr. Gilbert Levin included L-glucose in his Mars experiment?

To compare the taste of sugars

To test the effects of sugar on Mars soil

To provide a backup energy source

To test if Martian life preferred a different sugar

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following best describes a geometric isomer?

Molecules with identical spatial arrangements

Molecules with the same molecular formula but different connectivity

Molecules that are mirror images and non-superimposable

Molecules with double bonds and different group arrangements

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the term used for a pair of non-superimposable mirror image molecules?

Identical molecules

Enantiomers

Geometric isomers

Constitutional isomers

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the Cahn-Ingold-Prelog convention, what does the 'R' designation indicate?

Achiral molecule

No chirality

Right-handed configuration

Left-handed configuration

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the first step in assigning priority to groups around a chiral center?

Identify the group with the lowest atomic number

Identify the smallest group

Identify the group with the highest atomic number

Identify the largest group

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a quick trick to handle molecules where the lowest priority group is in the same plane as the chiral center?

Rotate the molecule 180 degrees

Invert the hydrogen with the group pointing back

Invert the molecule

Switch the highest and lowest priority groups

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What characteristic makes methylcyclopentane achiral?

Multiple chiral centers

Non-superimposable mirror images

Internal plane of symmetry

Presence of a chiral center

8.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How can you determine if a molecule with two chiral centers is achiral?

Check for identical chiral centers

Check for an internal plane of symmetry

Check for non-superimposable mirror images

Check for different atomic numbers

9.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the chirality of trans-1,2-dibromocyclohexane?

Achiral

Symmetrical

Chiral

Non-superimposable

10.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following molecules is likely to have enantiomers?

A molecule with identical groups

A molecule with no chiral centers

A molecule with one chiral center

A molecule with an internal plane of symmetry

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