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Q: 1-Chloro-1,2-diphenylethane can undergo E2 elimination to give either cis- or…
A: We'll answer the first question, since the exact one wasn't mentioned. Please submit the question,…
Q: draw 6 acyclic constitutional isomers of C6H12. Provide a name for each isomer, inclduing E-,Z-,R,S…
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- Compounds A and B are isomers having molecular formula C5H12. Heating A with Cl2 gives a single product of monohalogenation, whereas heating B under the same conditions forms three constitutional isomers. What are thestructures of A and B?4. Without consulting tables, arrange the following alkenes in order of increasing boiling point.Arrange the following alkenes in increasing stability.
- Give the series of reactions below, identify and give the iupac name for the following compounds, in short identify and name A,B,CWrite structures for products A, B, C, and D showinf stereochemistry. (Hint: B and D are stereoisomers)Dehydrohalogenation of 1-chloro-1-methylcyclopropane affords two alkenes (A and B) as products. Explain why A is the major product despite the fact that it contains the less substituted double bond.
- Explain the Mechanism - Addition of Dichlorocarbene to an Alkene ?a. How many vinylic hydrogens does cyclopentene have? b. How many allylic hydrogens does it have?Friedel–Crafts alkylation of benzene with (R)-2-chlorobutane and AlCl3 affords sec-butylbenzene.a. How many stereogenic centers are present in the product?b. Would you expect the product to exhibit optical activity? Explain, with reference to the mechanism.