Consider the reaction of 2,4-dimethyl-2-pentene with bromine in water. Part 1 of 2 Draw the bond-line formula for the product formed. Indicate stereochemistry where appropriate. B 0 Part 2 of 2 Click and drag to start drawing a structure. Give the IUPAC name of the final product. X 0 * C

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Q: Хо ОН 'CI

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A: concentration of methyl red (x axis) ) in terms…

Q: Thats very helpful thank you! How would this look in Aktiv format?

A: Product can be made by applying appropriate reaction mechanism.

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A: Correct answer is option C 2's complement conversion of 0300H content

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A: Given is organic compound. In MS spectrometry,  Base peak is tallest peak present in MS spectra.

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Q: 100 90 80 70 60 50 40 30 20 10 190 180 170 160 150 140 130 120 110 Structure:

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A: These can be calculated base on Woodward Fieser rules.

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A: Opt out the enantiomer of the given organic molecule.

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A: The solution is given below -

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A: A chiral centre is the carbon in which it is attached with four different substituents.

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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.