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What is the product from the reduction of the following molecule?
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- What steps are needed to prepare phenylacetylene, C6H5C = CH, from each compound: (a) C6H5CH2CHBr2; (b) C6H5CHBrCH3; (c) C6H5CH2CH2OH?Complete the following reaction equations :(i) C6H5Cl + CH3COCl →(ii) C2H5NH2 + C6H5SO2Cl →(iii) C2H5NH2 + HNO2 →I recovered 3 mL of water, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O.
- Virgin coconut oil contains about 46-48% of lauric acid (CH3(CH2)10COOH). In thepresence acid catalyst and an alcohol, propose the mechanism of this reaction.The product of the following reaction is __________ . Ph-N2+ + H3PO2 → Ph-PO2-2 aniline benzene nitrobenzene Ph-PO2H2Alcohols can undergo a lot of different reaction mechanims. If the alcohol group (OH) is attaached to an aromatic core, how will the chemistry change as compared to a typical alkyl alcohol? A) The OH group will become more polarised and more nucleophilic. B) The OH group will become more susceptible to oxidation C) The OH group will become more polarised and therefore basic D) The OH group will become more polarised and therefore acidic.
- Show how the synthetic scheme developed in Problem 23.67 can be modified to synthesize this triiodobenzoic acid X-ray contrast agent.select the most appropriate reagent(s) to effect the change. K2Cr2O7, H+ H2, Pd 1. Disiamylborane, 2. HO–, H2O, H2O2 NaOCl H2SO4, HgSO4The -N(CH3)3+ group is considered a .... Ortho/Para Directing Activator Ortho/Para Directing Deactivator Meta Directing Deactivator
- Give two syntheses for (CH3)2CH¬O¬CH2CH3, and explain which synthesis is betterMinor product via E1 for 2-butanol and HCl?When (CH3CH2)3CBr is added to CH3OH at room temperature, the product is (CH3O)C(CH2CH3)3. Propose a mechanism(s) for the reactions leading to these products and used curved arrows to show the movement of electrons.
