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Draw the products expected from the addition of Bromine (Br2) to 1-heptyne.
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Solved in 2 steps with 2 images
- Explain why α-pyrone reacts with Br2 to yield a substitution product (like benzene does), rather than an addition product to one of its C=C bonds.Draw structures of compounds that fit the following descriptions: a) An , unsaturated ketone, C9H8O b) An diketone c) An aromatic ketone, C9H10O d) A diene aldehyde, C7H8O4-pyranone will readily undergo an acid-base reaction. Identify the reaction conditions that will result in the formation of an aromatic product. Then, draw the aromatic resonance product structure. Include all lone pairs in your structure. Ignore inorganic byproducts. H3O+
- SN2 reaction is an example of a nucleophilic substitution reaction. Imagine that 1-iodobutane reacts with 4-methylheptan-1-ol under basic conditions. Draw the structure of the two reactants.Draw the structure of the chlorohydrin formed by treating 1-methylcyclohexene with Cl2/H2O.What reaction conditions are needed to convert (R)-2-ethyl-2- methyloxirane to (R)-2-methylbutane-1,2-diol ?
- Structure for 4-(2-methylbutyl)-N-(3-methylbutyl)aniline0 CH₂ → ?? If the above compound is subjected to combustion, what are the products? ethanoic acid +2-phenyl-ethene-1-ol 15CO₂ (g) + 5H₂0 (g) O 2-phenyl-ethyl-ethanoate + H₂O 20CO₂ (g) + 10H₂O(g) →?? CH, if the above compound was treated with H and H₂O what product will form?What reaction conditions are needed to convert (R)-2-ethyl-2-methyloxirane to (S)-2- methylbutane-1,2-diol ?
- What is the structure of C4H6 that can react with NaNH2 and CH3I? What is the product? What reagents are needed to turn this Product into Z-2-pentene?Draw the structure of the product formed when 1,2-diethylcyclopentene is treated with H2/Pd.The reaction of Hbr with 2-methylpropene produces 2-bromo-2-methylpropane. What is the structure of the carbocation formed during the reaction?