y clear The compound shown here can be prepared by reduction of what starting material? NH₂ Question 10 of 25 Search A) nitrobenzene B) aniline C) benzaldehyde D) phenol E) chlorobenzene
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- Provide reagents and reaction conditions for each stepShow how to Synthusize fon benzene and neassoy reogentsMelamine, used as a fire retardant and a component of the writing surface of white boards, can be prepared from s-trichlorotriazine through a series of SNAr reactions with ammonia. The first substitution takes place rapidly at room temperature. The second substitution takes place near 100 °C, and the third substitution requires even higher temperature and pressure. Provide an explanation fatr this reactivity.
- Give step-by-step mechanism for the following reactionprovide the major organic product3) Show how you would synthesize the following Compounds, storting with benzene or toluene ond ASSume any necessory pro duct (ond seperoble from ortho) in ortho, pora reogents, poro is the mogor mixture c)o- chlorobenzoic ocid d) m- chloronitro benzene
- Indicate the major organic product from the reaction shown. NH NABH3CNName and Draw the Phenolof all possible chemical (Electrophilic aromatic substitution) reactions of the compound namely; Halogenation (Chlorination or Bromination) NitrationProvide the mechanism for the following reaction (1) PhMgBr (2 equiv) (2) H3O+ workup OH
- b) The Wolf-Kishner reduction is a reaction used in Organic Chemistry to convert carbonyl functionalities into methylene group. The reaction was used to convert an aldehyde or ketone to an alkane using hydrazine, base and thermal conditions. The mechanism begins with the attack of hydrazine of the aldehyde or ketone. Stage 1: The reaction of aldehyde/ketone with hydrazine to produce hydrazine Stage 2: Reaction with the base and heat to convert hydrozone to alkane Write the mechanism of the reaction.explain which reagents and whyChoose which compound is more reactive when reacted with N2OH in water solvent and he reason clearly. vs OH HO,
