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Abstract: The purpose of this lab was to synthesize triphenylmethanol from benzophenone and bromobenzene by the formation of a Grignard compound with the reagents bromobenzene and magnesium metal. The bromobenzene was first transformed into the Grignard compound and was then reacted with the benzophenone to make the final product. The mixture was then mixed with sulfuric acid and the organic layer was extracted via a separatory funnel. The mixture was then recrystallized from methanol and was allowed. The condensation of dithio-oxamide with aromatic aldehyde was described by Ephraim. Multistep Synthesis of Tetraphenylcyclopentadienone In this laboratory experiment a synthesis was performed through several separate steps. The purpose of the experiment was to synthesize tetraphenylcyclopentadienone from benzaldehyde and to run reactions on carbonyl containing compounds. There was a total of three steps that led up to the synthesis of the final product, tetraphenylcyclopentadienone. The first step of the experiment was the condensation of benzaldehyde to yield.

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Acoustic Theory and Synthesis

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The Altmetric Attention Score is a quantitative measure of the attention Theor a research article has received online. Clicking on the Acoustic Theory and Synthesis icon will load a page at altmetric. Find more information on the Altmetric Attention Score and how the score is calculated. Interlayer charge-transfer CT excitons in heterostructures are of great importance because of their crucial roles in manipulating the device performance and many-body quantum behaviors.

The Grignard Synthesis of Triphenylmethanol

Photoelectron spectroscopies verify that the interlayer CT was promoted by the type-II energy band alignment. The American Chemical Acoutic holds a copyright ownership interest in any copyrightable Supporting Information. Acoustic Theory and Synthesis available from the ACS website may be downloaded for personal use only. Users are not otherwise permitted to reproduce, republish, redistribute, or sell any Supporting Information from the ACS website, either in whole or in part, in either machine-readable form or any other form without permission from the American Chemical Society. For permission to reproduce, republish and redistribute this material, requesters must process their own requests via the RightsLink permission system.

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