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- Provide the missing starting material, reactant or product. Show appropriate stereochemistry. a) b)• Same reagents as acid-catalyzed dehydration, except starting with a instead of an alcohol. • Same as the general mechanism hydrohalogenation, except with . Remember that EVERY acid-cat. mechanism begins with General Reaction: EXAMPLE: Provide H₂O H₂SO4 EXAMPLE: Provide the mechanism for the following addition reaction. H₂O H₂SO4 OH WH H₂O H₂SO4 as the nucleophile and ends with do PRACTICE: Provide the mechanism and predict the product of the following reaction. MAXOTrue/False question and multiple choice. explanatiom not needed. just give the answer. thank you. a) Williamson synthesis of ether requires un hindered alkyl halide and hindered alcohol b) NaBH4 can reduce a carboxylic acid to primary alcohol c) Conjugated diene reacts with which among the following to form a cyclohexene?1) Phenol2) Dienophile3) Hexane4) Tribromo phenol d) 1,3 -cyclohexadiene is 1. aromatic 2. has higher heat of hydrogenation than cyclohexene 3. is a good dienopile 4. has lower heat of hydrogenation than cyclohexene
- Topic: Reactions of benzene Starting from benzene, synthesize the following compounds. Write the complete reagent/s and intermediate product/s. The step by step mechanism (movement of arrow) is not necessary.can you solve 12.64. Devise a synthesis of (3R,4S)-3,4-dichlorohexane from acetylene and any needed organic compounds or inorganic reagents.C.) Obtain oxidation reduction products in four different ways using benzaldehyde and appropriate reagents and reactions.
- provide the mechanism given the product and starting material along with any reagents neededSelect the keyword or phrase that will best complete each sentence. Key terms: backside carbocation elimination frontside hyperconjugation inversion maintenance nucleophile product racemization stronger substitution weaker Alkyl halides undergo A orbital. reactions with Brønsted-Lowry bases. is a sp² hybridized and trigonal planar and contains a vacant p All SN2 reactions proceed with in attack of the nucleophile, resulting of configuration at a stereognic center. Spreading out charge by the overlap of an empty p orbital with an adjacent o bond is called Equilibrium favors the products of nucleophilic substitution when the leaving group is a base than the nucleophile. According the to Hammond postulate, the stability of the determines the rate of its formation. The formation of equal amounts of two enantiomeric products from a single starting material is called A is an electron-rich compound, which donates a pair of electrons to an electron deficient compound, forming a covalent bond.…Supply the missing reagent for the following reactions.
- 6) Develop a series of reactions we have covered in lecture that would produce the following molecules. Use any reagents necessary, but you must start with an alkene with one double bond (any alkene you choose) as one of your reactants. онThe reaction below could run through both substitution and elimination reactions. 1. Provide the correct reagent to produce the products shown 2. State which mechanism(s) was followedSynthesize each compound from acetylene. You may use any other organic or inorganic reagents.1. CH3CH2CH2CH2CHO2. CH3CH2CH2CCl2CH3 Please explain how you arrived at the answer; I don't understand this. Thank you!