Propose a structure for an alkyl halide that generates only (Z)-3-methyl-2-phenylpent-2-ene upon E2 elimination with NaOH. Include: The curved arrows to show the mechanism of the transformation The IUPAC name of the proposed starting material (including stereocenters) NaOH alkyl halide (Z)-3-methyl-2-phenylpent-2-ene IUPAC name of alkyl halide:

Q: draw the major organic products the student would expect from their mechanism. Be sure to use wedge…

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Q: Consider the reaction of an alkyl bromide with water. Draw the neutral organic products. Br H₂O…

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A: Concerted mechanism is the mechanism in which bond breaking and bond making occurs in a single step.

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Q: The radical addition of HBr can be used to cyclize a Br carbon chain. Provide a detailed mechanism…

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Q: please solved it correctly?   all mechanism and all steps.

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Q: Show product and provide mechanism NO2 LiAlH4 THF, RT LiAlH4 THF, RT

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Q: Draw the starting alkyne that would lead to this major product under these conditions. Drawing HBr…

A: When alkyne reacts with excess HBr it produce geminal  dihalide .Hence, substrate must be Alkyne .

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Q: Draw a reasonable mechanism for the following reaction: H heat H-CEC-CH3 Br2 H-CEC-CH,Br C=C=C Br

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Q: Identify the major and minor product(s) that are expected for the following reaction. Select all…

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A: Carbon-containing two ester groups R2C(OR')2 is known as an acetal.

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Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.