What bromo-substituted compound would be required to react with (CH 2 =CH) 2 CuLi in order to form each of the following compounds? b.

Hello, everyone. Today, we have the following problem, determine a chloral substituted compound that will react with the following organo cate compound to form the following product. So this described reaction is a coupling reaction with a Guillain reagent. And so we need to examine the product. We need to note that it only contains or the alky group contains a beetle group. So this means that the beetle group must have come from the following. So we draw pick structure that contains the alkene. And we see that our organo coup rate or the Gilman region contains two equivalences of propal groups attached to a copper. So it essentially has the following structure and our coup ate our copper is negatively charged and then our lithium is a positively charged spectator ion. And what will occur is we have a nil attack then its organo and since our organo it has three carbons and our product has four, we simply need to have a chloral substituted product with one carbon as follows. And so with that, we have solved the problem overall, I hope it helped. And until next time

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13. Alcohols and Carbonyl Compounds

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Problem 7b

Textbook Question

What bromo-substituted compound would be required to react with (CH₂=CH)₂CuLi in order to form each of the following compounds?
b.

Verified step by step guidance

Step 1: Analyze the target compound provided in the image. The compound consists of a cyclohexane ring attached to a chain containing two double bonds (CH2=CH groups). This suggests that the reaction involves the addition of a vinyl group to a bromo-substituted compound.

Step 2: Understand the role of (CH2=CH)2CuLi. This reagent is a Gilman reagent, which is commonly used in organic synthesis for coupling reactions. It reacts with alkyl halides (such as bromo-substituted compounds) to form new carbon-carbon bonds.

Step 3: Determine the structure of the bromo-substituted compound required for the reaction. To form the target compound, the bromo-substituted compound must have a cyclohexane ring with a bromine atom attached to the position where the vinyl group will be added.

Step 4: Predict the reaction mechanism. The Gilman reagent (CH2=CH)2CuLi will replace the bromine atom in the bromo-substituted compound with a vinyl group (CH2=CH). This substitution occurs via a nucleophilic substitution mechanism.

Step 5: Conclude the structure of the required bromo-substituted compound. The compound should be bromocyclohexane, as the bromine atom is positioned on the cyclohexane ring where the vinyl group will be introduced.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Bromo-Substituted Compounds

Bromo-substituted compounds are organic molecules that contain a bromine atom attached to a carbon chain. These compounds are often used in nucleophilic substitution reactions, where the bromine atom can be replaced by a nucleophile. Understanding the structure and reactivity of these compounds is essential for predicting the products of reactions involving them.

Organocuprates

Organocuprates, such as (CH2=CH)2CuLi, are organometallic reagents that contain a copper atom bonded to an organic group. They are known for their ability to act as nucleophiles in reactions with electrophiles, such as bromo-substituted compounds. The reactivity of organocuprates allows for the formation of carbon-carbon bonds, making them valuable in organic synthesis.

Nucleophilic Substitution Reactions

Nucleophilic substitution reactions involve the replacement of a leaving group (like bromine) in a molecule with a nucleophile. These reactions can follow different mechanisms, such as SN1 or SN2, depending on the structure of the substrate and the conditions of the reaction. Understanding these mechanisms is crucial for predicting the outcome of reactions involving bromo-substituted compounds and organocuprates.

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