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3. the stereospecificity of today’s bromination reaction induces the reaction to yield only one of the following products: meso or how are the meso and racemic products related? they are [Select ] . 4. What experimental data did you collect to verify the stereospecificity of this bromination reaction [ Select ]

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User NiMux
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Final answer:

A stereospecific reaction selectively reacts with one stereoisomer and produces one stereoisomer in the product. The meso and racemic products are related in terms of their optical activity.

Step-by-step explanation:

A stereospecific reaction is one that selectively reacts with one stereoisomer among the reactant and produces one stereoisomer in the product.

In the case of today's bromination reaction, it is stereospecific and yields only one product.

The product can be either meso or optically active, depending on the reactant used.

The meso and racemic products are related in that they both consist of a mixture of enantiomers.

Meso compounds have an internal plane of symmetry, meaning that even though they have multiple stereocenters, they are optically inactive.

Racemic compounds, on the other hand, do not have a plane of symmetry and therefore they are optically active, but their activity cancels out due to the equal amounts of both enantiomers present.

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User Fernyb
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Final answer:

The bromination reaction can yield either meso or racemic products. Stereochemistry techniques can be used to verify the stereospecificity of the reaction.

Step-by-step explanation:

In today's bromination reaction, the stereospecificity induces the reaction to yield only one product. This product can be either meso or racemic. Meso compounds have an internal plane of symmetry, which means they are achiral. Racemic compounds, on the other hand, have equal amounts of both enantiomers and are optically inactive.

Experimental data can be collected to verify the stereospecificity of the bromination reaction by analyzing the stereochemistry of the product using techniques such as NMR spectroscopy or X-ray crystallography. These techniques can provide information about the spatial arrangement of atoms in the molecule and determine if the reaction is yielding predominantly one stereoisomer.

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User Sten Petrov
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