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How may methyl bromide be preferentially converted to methyl isocyanide?
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- What is a reasonable synthetic pathway on how benzoyl chloride can be synthesized to form N-(2-phenylethyl) aniline?what would a detailed step-by-step mechanism be for a reaction between bromine and trans-stilbene if the solvent, ethanol, is a stronger nucleophile than the bromide ions?Define the Reaction of Organometallic Reagents with Other Compounds ?
- Fill in the blanks A primary arylamine treated with nitrous acid is converted to a arenediazonium salt whose___ part is a___ leaving groupin a reaction where trans-stilbene reacts with a molecule of bromine while using ethanol as a solvent, what would happen if the ethanol was a more reactive nucleophile than the bromide ion(s)? would the product be affected?Could you summarize the main characteristics of nucleophilic acyl substitution?
- Give an explanation for the observed stereoselectivity in the following reaction.which statement is true in the e2 reaction of the given compounds with NaOCH2CH3?The SN2 reaction can be carried out intramolecularly (in the same molecule). What product do you expect to form when treating 4-Bromo-1-butanol with a base?justify the reason
- Which solvent would make the bromination through electrophilic aromatic substitution faster? Pentane Toluene Propanoic acid Petroleum etherArrange these compounds in increasing order of reactivity in SN2 nucleophilic substitution?p-Fluoronitrobenzene is more reactive toward hydroxide ion than is p-chloronitrobenzene. What does this tell you about the rate-determining step for nucleophilic aromatic substitution?