#53 The retro synthetic approach for this molecule
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#53 The retro synthetic approach for this molecule
Step 1
The molecule is as follows:
Step 2
The retro synthetic approach for this molecule is shown below.
Step 3
Therefore, the preparation of this molecule can be achieved by the following steps:
Step1: First there is Diels alder reaction takes place between 1,3-butadiene and bromoethene.
Step 4
Step2: The resultant product is treated with magnesium in dry ether condition to form aryl Grignard reagent.
Step 5
Step3: Then this aryl Grignard reagent react with butanone and formed product and again this product react with water to formed final product as shown:
Get the Free Online Chemistry Q&A Questions And Answers with explain. To crack any examinations and Interview tests these Chemistry Questions And Answers are very useful. Here we have uploaded the Free Online Chemistry Questions. Here we are also given the all chemistry topic.
ChemistryExplain team has covered all Topics related to inorganic, organic, physical chemistry, and others So, Prepare these Chemistry Questions and Answers with Explanation Pdf.
Question
#53 The retro synthetic approach for this molecule
Answer
Step 1
The molecule is as follows:
Step 2
The retro synthetic approach for this molecule is shown below.
Step 3
Therefore, the preparation of this molecule can be achieved by the following steps:
Step1: First there is Diels alder reaction takes place between 1,3-butadiene and bromoethene.
Step 4
Step2: The resultant product is treated with magnesium in dry ether condition to form aryl Grignard reagent.
Step 5
Step3: Then this aryl Grignard reagent react with butanone and formed product and again this product react with water to formed final product as shown:
Labels: Q&A Organic Chemistry
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