Consider the following reaction: Part 1 of 3 WOH HI By which principal mechanism will the reaction shown proceed? Select the single best answer. SN 1 SN 2 Part 2 of 3 How many major organic products, including stereoisomers, will be produced by the reaction shown? Select the single best answer. 1 2 E Part: 2/3 Part 3 of 3 Draw the structures for the major organic product(s) of the reaction shown.
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considering a following reaction. Draw the structures for the major organic product(s)of the reaction show.
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- Can I have some help with this questionThe following chemical reaction is used to synthesize a flavouring agent that has an aroma similar to bananas. H₂SO4(aq) CH3COOH(1) + CH3(CH₂)₂OH(1) I || Identify the type of reaction that is represented by this synthesis. Select one: CH₂COO(CH₂)₂CH₂(1) + H₂O(1) IV O addition O hydrogenation O substitution O esterification O elimination10. What is the major organic product generated in the reaction below? HO HO 40||!!!!!! (A) OH ...... (B) 1) 03 2) (CH3)2S HO O (C) H НО. (D)
- Q2- Which one of the following reaction is unreasonabl? A) NaOH(aq)+HCl(aq)-NaCla+H₂O B) H2(g)+1/202)→ H₂Op AHneutralization=-851.5kJ/mol =-283.5kJ/mol AHormation C) CH3COOH + H₂O-CH:COO(g) + H AHassociation = +213.5kJ/mol D) Mg(+2HCl → MgCha) + H₂ - AHformation =+315.5kJ/mol Q3- If A 25.0 mL of diluted bleach solution has required 30 mL of 0.30 M Na S,O; to reach the endpoint of the titration. Calculate the mass percent of NaCIO in the original sample (Molar mass NaCIO = 74.5 g/mol). Assume the density of bleach solution is 1.084g/mL and the dilution factor is 10. B) 9.96% C) 0.996% D) 12.4% A) 19.92% and the coloDraw the structure of the major organic product of the reaction. col CI / 1. LIAIH4, ether 2. H30+ • You do not have to consider stereochemistry. t √ [F ? Ⓡ ChemDoodleCH3 CH3 Br- Br2 .CH3 CH2Cl2 CH3 H3C H3C Br Electrophilic addition of bromine, Brɔ, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH,Cl,. In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions CH3 CH3 CH3 CH3 H3C H3C :Br: :Br:
- Give the major organic product of the following reaction. NaOCH NaOH 0 ? CH₂OH H₂O heat கு OMe OH these conditions or the correct product is not listed here. OMeDon't use hand raiting pleaseH3C CH3 H3C NA C→XT Br Br₂ CH₂Cl₂ H3C Electrophilic addition of bromine, Br₂, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH₂Cl₂. CH3 Br In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Br CH3 H3C CH3