What are Grignard reagents, and why are they important?
Grignard reagents are organomagnesium compounds used to form carbon-carbon bonds, essential for synthesizing alcohols, carboxylic acids, and hydrocarbons due to their strong nucleophilic nature.
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What roles do bromobenzene, magnesium, and diethyl ether play in a Grignard reaction?
Bromobenzene forms the phenyl group for the Grignard reagent, magnesium facilitates the carbon-metal bond formation, and diethyl ether stabilizes the Grignard reagent and acts as a solvent.
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What is the difference between oxidation and reduction reactions?
Oxidation is the loss of electrons, typically adding oxygen or removing hydrogen; reduction is the gain of electrons, typically adding hydrogen or removing oxygen.
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What are the main reagents used in oxidation and reduction reactions in the lab?
Oxidation uses sodium hypochlorite (NaOCl); reduction uses sodium borohydride (NaBH₄) or lithium aluminum hydride (LiAlH₄) as a stronger reducing agent.
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What is the difference between kinetic products and thermodynamic products?
Kinetic products form quickly with lower activation energy but are less stable; thermodynamic products form slowly with higher stability and require higher temperatures.
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Which product, endo or exo, is the major product in a Diels-Alder reaction and why?
The endo product is the major product due to secondary orbital interactions that stabilize the transition state, following the endo rule.
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What is the Diels-Alder reaction?
It’s a [4+2] cycloaddition reaction between a diene and a dienophile, producing a cyclohexene derivative by forming two new carbon-carbon sigma bonds in a concerted, stereospecific manner.
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Why is the Diels-Alder reaction a syn addition?
Because the reaction is concerted, all new bonds are formed on the same face of the reactants, resulting in stereospecificity.
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Does the Diels-Alder reaction have stereoselectivity?
Yes, it exhibits high stereoselectivity and regioselectivity due to its concerted mechanism, preserving the stereochemistry of the reactants.
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How do you calculate the theoretical yield of a reaction?
Determine moles of the limiting reactant, use the stoichiometry of the reaction to calculate moles of product, and convert moles of product to grams using molar mass.
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How do you calculate the percent yield of a reaction?
Percent Yield = (Actual Yield / Theoretical Yield) x 100.
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What is the purpose of glacial acetic acid and anhydrous sodium sulfate in lab reactions?
Glacial acetic acid enhances reaction efficiency by providing an acidic medium; anhydrous sodium sulfate removes residual water during the workup step.
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How does water affect the melting point of semicarbazones?
Water lowers the melting point by introducing impurities, disrupting the crystal lattice structure.