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- Identify the principal organic product in each case NaH CH3C .OH 7It is a type of organic reaction in which parts from two molecules exchange. * Elimination Substitution Addition Rearrangement In the reaction given below, what type of addition reaction is used? * H H H H H-C-c=C HBr н-с — с — С —с —н + H H H Br H O Hydrogenation O Hydrohalogenation O Halogenation O Dehalogenation H-O-ISynthesize each compound from benzonitrile (C6H5CN) as the only organic starting material; that is, every carbon in the product must originate in benzonitrile.
- 7 Identify the functional group and the IUPAC name for each of the three compounds in the reaction below: H₂SO4(aq) Compound 1 CH₂COOH (1) + CH₂(CH₂)₂OH(1) I || || Functional Group carboxyl hydroxyl Ester linkage + CH3COO(CH₂) CH₂(1) + H₂O(1) IV III IUPAC Name → + +5B In the following reactions, mixtures of alkenes and ethyl ethers are formed. Draw their structures. Explain which is or are likely to be the main product(s) in each reaction. In case of formation of two isomers of alkenes, explain which is formed in greater proportion CH3 CH3 H3C-C H -Br CH3 EtOHWhat is the systematic name of the product P of this chemical reaction? 0 OH HỌ—CH2 CH OH O | CH || -C-OH + KOH X P + H₂O Ś
- What is the major products formed when benzene reacts with the following : 1- chloro-2,2-dimethylpropane + AICI, 2- Fuming H,SO4 3- Iodine + CuCl2 US X x i BI !!An important step in one synthesis of carboxylic acids is the deprotonation of diethyl malonate and its alkyl-substituted derivative: Base CH;CH2O OCH,CH3 CH;CH,0 OCH2CH3 H2 Diethyl malonate Base CH;CH,0 °C `OCH,CH3 CH;CH,O OCH,CH3 R Alkyl substituted diethyl malonate NaOH can deprotonate diethyl malonate effectively, but NaOC(CH3)3 is typically used to deprotonate the alkyl-substituted derivative. Explain why.Q2. Provide the reagents O OMe OMe CO₂Me CO₂Me
- During multistep syntheses, reduction reactions are often performed. Functional groups react differently with these reagents. With this in mind, draw the structure of the product of this reaction: CO₂H CO₂H s HO₂C • For your convenience, the starting material has been drawn for you in the sketchpad. HO OH LIAIH4 -OH - [ ] ?t3u0k A HBMethyl isocyanate, CH3 -N= C = O, is used in the industrial synthesis of a type of pesticide and herbicide known as a carbamate. As a historical note, an industrial accident in Bhopal, India, in 1984 resulted in leakage of an unknown quantity of this chemical into the air. An estimated 200,000 people were exposed to its vapors, and over 2000 of these people died. Q.) Methyl isocyanate reacts with strong acids, such as sulfuric acid, to form a cation. Will this molecule undergo protonation more readily on its oxygen or nitrogen atom? In considering contributing structures to each hybrid, do not consider structures in which more than one atom has an incomplete octet