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- What is the major substitution product of the following reaction? Br NaOH ? heat ОН Br Br ОН (A) (B) (C) (D) O A O B ODWhat is the major product for the following reaction? SO₂H-O OC O a Od Ob X De MeOH [H₂SOA] m MeO enant I {-x {- OMe enantThe pKa of p-cyclopropylbenzoic acid is 4.45. Is cyclopropylbenzene likely to be more reactive or less reactive than benzene toward electrophilic bromination? Explain.
- Melamine, 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.What is the major organic product obtained from the following reaction? CI O O CH,COONa DMSO OMe OCOMe OH OHAnswer the following questions based on the given reaction scheme: A OH он So;Na conc. H,SO, NaOH ŠO,Na Br C он OH он Br acid Br SOgNa Br 200 °C H,SO, SO,Na Which step(s) require heating? DA OB OC OD OE In which step(s) does aromatic halogenation occur? DA OB OC DE In which step(s) does aromatic sulfonation occur? DA OB OC OD OE What is the name of the product?
- the structure of the major product of the following reaction is NaCN Br DMF CN CN CN A Oc OA 3.12:04 PM Tue Apr 25 < S T List the reagents to achieve the synthesis o-oi حمد он ●●● Ď 78% + : 1 1 2 (+)Identify the suitable reagents for the given reaction and arrange them accordingly. 1 OH OEt 2 OEt OEt O 1) EtOH, H₂SO4; 2) EtOH, H₂SO4 O 1) EtONa followed by H₂O; 2) TsCl/py followed by EtONa O 1) EtONa followed by H₂O; 2) NaH followed by EtBr O 1) EtOH, H₂SO4; 2) NaH followed by EtBr O 1) EtOH, H₂SO4; 2) TsCy followed by EtONa
- Which compound is the dominant product of the reaction below? EN CH;CN OH OH HO CN CN HO. CN Compound A Compound B Compound C Compound D Compound B Compound C Compound D Compound AStep 2: A hemiacetal formation has a similar mechanism to the hydrate reaction, except 1 equivalent of alcohol is added instead of water. 1² R₂ R₁ LOR3 R₁ R₂ The hemiacetal reaction is also reversible and can also be catalyzed by either acid or base. Hemiacetals are not usually isolated, except in the formation of 5- and 6-membered rings, as often seen in carbohydrate chemistry. Identify the hemiacetal formed from the intramolecular cyclization of the molecule shown. OH H OH R3OH OH OH OH CH₂OH NaOH ?5- Provide a concise synthesis for the following compound starting from benzene: Orther IPSO SO₂H ortho Para meta CI NO₂