Interpretation: The reason behind no immediate separation of solid when bromine solution is added to solution of
Concept introduction:Alkenes are considered electron-rich and undergo bromination addition reaction with
The mechanism of
In the second step, the strained bromonium ion intermediate opens while
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Experimental Organic Chemistry: A Miniscale & Microscale Approach (Cengage Learning Laboratory Series for Organic Chemistry)
- please help me - pleasearrow_forwardFor extraction with ethyl-4-aminobenzoate and naphthalene using dichloromethane as the solvent, how does one separate the two compounds from one another?arrow_forwardConsidering the stoichiometry of the reaction (balance the equation!), what is the net oxidation state difference of the carbons in benzophenone going to benzopinacol? Remember that you have to calculate the oxidation state of the carbons in the product (benzopinacol) and subtract the oxidation state of the carbons in the reactants (benzophenones). The shortcut is to only calculate the oxidation states of the carbons that seem to have changed their bonding. Give a whole number answer with no units. hv OH Ph Ph OH Ph' Ph' Ph Ph OH Answer: -1arrow_forward
- explain some of the hazards (name at least three) involved in the Friedel-Crafts Acylation: Synthesis of 4-methoxyacetophenone from anisole experiment. What are some necessary safety precautions when working with aluminum chloride? List compounds that react in a hazardous manner with aluminum chloride and are therefore incompatible. What hazardous by-products are formed in this experiment? Why is it necessary to perform this experiment in the fume hood?arrow_forwardWhat product would you obtain if you evaporated the water from the NaOH layer prior to acidifying the layer? (we are trying to extract p-tert-butylphenol; it is in aqueous solution with NaOH, which we used to extract it from a mixture dissolved in ether). Prior to acidifying with HCl, it is ionic (phenoxide).arrow_forwardWhich experimental method would you recommend for the preparation of 1-bromooctane and of t-butyl bromide?arrow_forward
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- Please answer the questions in the imagearrow_forwardIn the synthesis of dibenzalacetone, what is the purpose of swirling the flask for 20 mins? It makes the benzaldehyde more electrophilic It removes the excess acetone in the mixture. It prevents the formation of side products It allows for the evaporation of ethanol, leaving water as solvent where the product is insoluble.arrow_forward1. Occasionally, a crossed Cannizzaro reaction is carried out to reduce benzaldehyde derivatives to the corresponding benzyl alcohol, utilizing formaldehyde as the reducing agent. i) Please show the mechanism by which this occurs.arrow_forward
- EBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENTMacroscale and Microscale Organic ExperimentsChemistryISBN:9781305577190Author:Kenneth L. Williamson, Katherine M. MastersPublisher:Brooks Cole