(D)SN2-substitutionacid-catalyzed hydrolysis(E) The m addition-eliminationallylic halogenationhalohydrinationinternal displacementLindlar reductionaddit/.S₁1-substitutionSubmit Ansv SN2-substitutionvinylic halogenation۵۰ +H₂H₂-OHH₂?nore oupChemDoodleⓇroduct, 1,2,3-propanetriol, is:ing Following are the steps in the industrial synthesis of glycerin.NaOH, H₂O B (C₂H₂O)CH₂=CHCH,PropeneCl₂A (C₂H₂CI)heatC (C₂H,ClO₂)Ca(OH)2, D (C3H6O2)heatCl₂, H₂OH₂O, HCIOHHOCH₂CHCH₂OH1,2,3-Propanetriol(glycerol, glycerin)

The given example are a addition and substitution reaction

(D) **** SN2-substitution Submit Ansv ۰/, acid-catalyzed hydrolysis (E) The m addition-elimination allylic halogenation halohydrination addit internal displacement Lindlar reduction S₁1-substitution SN 2-substitution vinylic halogenation مر H₂H₂-OH H₂ nore sup ? ChemDoodle roduct, 1,2,3-propanetriol, is: ing

(D) **** SN2-substitution Submit Ansv ۰/, acid-catalyzed hydrolysis (E) The m addition-elimination allylic halogenation halohydrination addit internal displacement Lindlar reduction S₁1-substitution SN 2-substitution vinylic halogenation مر H₂H₂-OH H₂ nore sup ? ChemDoodle roduct, 1,2,3-propanetriol, is: ing

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Please complete boxed reactions. Thanks. P.s. this is not graded work but a study guide.
2. For each reaction, give the expected substitution product and predict whether the mechanism will be first order (Sw1) or second order (Sw2): a) 2-chloro-2-methylbutane + CH;COOH b) isobutyl bromide + NƏQME, c) 1-iodo-1-methylcyclohexane + CH;CH;OH
Markovnikov's Rule is needed to predict that the major substrate product in the reaction between HBr (hydrobromic acid) and will be O 2-pentene; 1-bromopentane 1-octene; 2-bromooctane O benzene; bromobenzene 3 of these 4 responses are correct O 1-pentene; 1-bromopentane
c) Complete the following reaction scheme for structures E, F, G, H and I. F Br2 / H20 Cl i. BH3, THF ii. H2O2 / H* КОН E G i. Оз ii. (CH3)2S H + I
The reaction of trichloroethanal with water is a nucleophilic addition reaction. It can be catalysed by small amounts of hydroxide ions, OH-. Complete the diagram below to suggest a mechanism for this reaction. Show all the relevant dipoles and curly arrows. Cl CI C C CI TO O H H CI O CI CI-C-C-H H O H The recommended adult dose of chloral hydrate as a sedative is 250 mg, three times a day. Calculate the mass of trichloroethanal you would need to react with water to make one week's supply of chloral hydrate for an adult, assuming a 60% yield. M₁: chloral hydrate, 165.5; trichloroethanal, 147.5
-a, B-unsaturated ketones, aldehydes react with nucleophiles 1,2-addition (direct addition): by R-MgX, LiAlH4 1.4-addition (conjugate addition): by R₂CuLi (Gilman reagent), and most other nucleophiles 1) (CH3)2CuLi 2) H* + 1) -MgBr 2)H₂O+
Researchers have been able to conduct sequential ring closing metathesis tollowed by a cross-metathesis reaction, in an effort to create rings and add carbons. However, cross-metathesis can be challenging when there are strained alkenes present, as shown in this example with a final product of 8%. Fill in the missing structures from each reaction. OBn OBn OBn Ru Ph C33H3605 A ACO Ru Ph ŌAC C39H4409 B
This requires multiple answers.
Q1// Prepare 2-methyl butane from 1-Chloro-2-butane by reduction alkyl halide ; using any material and catalyst that you needed ? writ the IUPAC name for all compounds ?
36) [ saturated / unsaturated ] alkane-like carbon compound. are known as compounds with the -OH group attached to an otherwise 37) The the >[ hydroxyl / oxonium / peroxy acid ] group primarily on the less substituted carbon. -catalyzed ring opening of an epoxide that has a tertiary carbon leads to formation of 38) If CH3CH2BR and an [ addition / elimination / oxidation ] reaction with a carbony! group. are reacted in pure ether, the resulting Grignard reagent can be used in 39) Assuming all structures below are planar, circle only the aromatic compounds (+1 or -1 per structure HOH 40) In terms of energy: a) Antiaromatic compounds are [ lower/ higher / identical ] to the corresponding open chain form with an equal number of carbons and
(a) In an acid-catalyzed hydration, one of the following 10 carbon alkynes is expected to produce a single hydration product? Select the correct alkyne and draw the structure of the hydration product that is formed from this alkyne. (I) 2-decyne; (II) 3-decyne; (III) 4-decyne; (IV) 5-decyne; (V) none of these will give a single hydration product. (b) The reaction shown below gives Compound X as the major product. The mass spectrum of X is shown. Br2, H20 Compound X 100 - MS-IW-5644 80 60 40 - 20 - 20 40 60 80 100 120 140 160 180 200 220 m/z Considering the reactions of alkynes and the MS data, de duce which of following structures corresponds to X: Br Br HO, IV V I II II Support your answer with a reaction mechanism for fomation of X and identification of relevant peaks in the mass spectrum. 12 Relative Intensity
Do not give handwriting solution.