How many stereocenters does sucrose, also known as table sugar, have? HO H OH HO H Н Н ОН Н. н OH OH OH H OH

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### How Many Stereocenters Does Sucrose, Also Known as Table Sugar, Have?

The image above shows the molecular structure of sucrose, commonly referred to as table sugar. Sucrose is composed of glucose and fructose units. It's crucial to understand the concept of stereocenters, which are atoms in a molecule bonded to four different groups, allowing for isomerism based on different spatial arrangements.

In the chemical structure of sucrose, there are multiple stereocenters, indicated by carbon atoms connected to different atoms or groups. Identifying these stereocenters is essential in organic chemistry as they contribute to the molecule's optical activity and chemical behavior.

To count the stereocenters: 
- Examine each carbon atom in the saccharide rings.
- Identify those bonded to four distinct groups.

In sucrose, each carbon atom that meets this criterion of being bonded to four different groups is considered a stereocenter, contributing to the molecule's chiral properties.
Transcribed Image Text:### How Many Stereocenters Does Sucrose, Also Known as Table Sugar, Have? The image above shows the molecular structure of sucrose, commonly referred to as table sugar. Sucrose is composed of glucose and fructose units. It's crucial to understand the concept of stereocenters, which are atoms in a molecule bonded to four different groups, allowing for isomerism based on different spatial arrangements. In the chemical structure of sucrose, there are multiple stereocenters, indicated by carbon atoms connected to different atoms or groups. Identifying these stereocenters is essential in organic chemistry as they contribute to the molecule's optical activity and chemical behavior. To count the stereocenters: - Examine each carbon atom in the saccharide rings. - Identify those bonded to four distinct groups. In sucrose, each carbon atom that meets this criterion of being bonded to four different groups is considered a stereocenter, contributing to the molecule's chiral properties.
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