NH,7.4- hydroxy – 3 -pentylanilineOHNH.8.1- aniline - 4 – iodobenzoic acid-cooHAuthored by: Sensei Wilmark Palacios9.o- chlorobutylbenzeneCatr10.3 - ethylanisole-COH II.Explain in your own words any mistake in the following given. The same construct of sentenceswith your classmates is up for deductions.NO1.m - nitrotoluene2- methyl - 3 – nitroanisole3.1- phenylhexaneAuthored by: Sensei Wilmark Palacios4.NOz3- chloro - 2- methoxy – 5 - nitroanisoleCOHCOH5.4- bromo – 3 – fluoro – 1- nitrobenzeneNO2HN6.2- methyl – 1- aminobenzene

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Answered: I. Explain in your own words any…

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...

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H3C₂ Br H₂O a. Enantiopure (1R, 3R)-3-Methylcyclohexanol b. Achiral 1-Methylcyclohexanol C. Racemic mixture (1R, 3R)- and (1S, 3S)-3-Methylcyclohexanol d. Diastereomeric mixture of (1R, 3R)- and (1S, 3R)-3-Methycyclohexanol
Which of the following provides a synthetic route to convert 3-iodo-2-methyl-1- butene into 2-methyl-2-butene? 1. NaOH; 2. H₂, Pt 1. H₂, Pt; 2. Br2 1. H₂, Pt; 2. NaOEt 1. H₂, Ni₂B; 2. KOtBu 1. H₂, Pt; 2. KOtBu
1) 1544565- NH₂ 2) CI of & 7) 8) reagents used: FeCl3/Cl₂ HNO3/H₂SO4 MeCI/AICI3 ACCI/Et₂N SO3/H₂SO4 Pd/C, H₂ NaOH H₂SO4/heat ACCI= CI [Choose ]
Name the following compound: O A. 3-methoxyhex-3-ene O B. (Z)-4-methoxyhex-4-ene O C. (E)-3-methoxyhex-3-ene O D. (cis)-3-methoxyhex-3-ene O E. (Z)-3-methoxyhex-3-ene
Q1. Give the structure(s) of the major organic produc(s) of A-H, Show stereochemistry if appropriate. Hz. Pd/C KMnO4. H0. B 1. BH, C 2. NoOH, H,02 C2. CH,OH D HCI E KI, H;PO, KMno HO". G H.
2. Sketch the proper structure (including stereochemistry) for each compound. a. (4R)-3,4-diethyl-4-methylheptane b. (5S, 7R)-7-chloro-2,4,4,5,7-pentamethyldecane C. (65, 75)-3,7-dibromo-3-ethyl-6-methylnonane
(1) Complete the following reactions with the proper structures: CH212 Zn (Cu) a- diethylether b- LiCu(CH;CH,CH2)k CH3 1. liquid ammonia + NaCECH 2. H30* 1. Mg, Ether Br d- 2. H2C=O 3. Нао* Cl2(PCY3)2Ru=CHC&H5 е.
Please help with the following... Draw the bond line structured for the reactants and the products obtained in the following reactions: 1. m-tertbutyl benzoic acid + 3-methyl-1butene, HF 2. 3-chloro-2,6-dinitrotulene + sodium ethoxide, ethanol 3. o-methylanisole + isobutanol, BF3
NH₂ NHỊCH, tipy (a) acrylamide Diamines are used as the building blocks for the synthesis of pharmaceuticals and agrochemicals. In the above synthesis, draw the structure of the product (b). ChemDoodle 1. LIAIH 2. H₂O • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Include cationic counter-ions, e.g., Na* in your answer, but draw them in their own sketcher. OF (b) 6
reactions. Be sure to show any significant stereochemical details. (a) I. Nall. CS 2. CH,I 3. heat (b) 1. BULI, LICI 2.MeCu(CN)LI (c) CH, Zn-Cu CH,l,, ether (d) CH,CO,H LOET (e) Br Zn, THO.
Q1/Do as required: 1-The role of H2SO4 in Preparation of Nitrobenzene. Explain 2- Preparation of Nitrobenzene in cool phase. 3-In an experiment Hydrolysis of Acetanilide What color does the litmus paper change to and why? 4-When acetanilide reacts with bromine (x), acctanilide gives p-bromo acetanil 5- why used strongly alkaline (NaOH)in Preparation of Aniline?
An organic chemistry student reacted benzene (excess) with a racemic mixture of (S) and (R) enantiomers of 2-chloro-3,3-dimethylbutane in the presence of AICI3 followed by water. Which of the following represents at least 50% of the final product profile? [Note: more than one answer may or may not apply.] ok of d b a ok *** CI f

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