Exp 11 (CHEM3105)

4G 08:44 The following presented reaction scheme lead to the synthesis of which major product from benzene, assuming separation of products is possible? So 1 HaOH Product CI Product HSO. 2 H,0 FeCl GA Meta-Chlorophenol U& para-ChloroSulfenic acid 4C Para Chiorophenol Da Meta-chloroaniline Add a caption... > Status (Custom)

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 → + +

Can you explain it? Provide examples with the various steps and explanations. How halogens affect the boiling/melting point? Does number of halogens affect it? For example, Ch3-Ch3 vs Ch3-Br vs Br-Ch3-Br

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From the table of available reagents select the one(s) you would use to convert:3-pentanol to 3-bromopentane:cyclopentanol to trans-2-methylcyclopentanol:Use the minimum number of steps; in no case are more than four steps necessary.List reagents by letter in the order that they are used; example: fa.

Starting Materials CH3B CH3CH2BR CH3CH2CH,Br C6H5Br Reagents Mg, ether 1. a. 2. 13CH2-13C-OH b. 13CO2 then H3O* 3. LIAIH4 then H3o* PBr3 CO2 then H30* C. 4. d. 5. C6HsCH2Br е. Select a starting material and a series of reagents necessary to synthesize this compound in as few steps as possible. Enter your selection as a number for the starting material, followed by the letters of the reagents, in the order that you wish to use them, i.e. 3abcf.

Subject:- Chemistry

what is the product(s) of the reaction of p-bromoaniline with HNO2, H2SO4, then CuCl and HCl

Macmillanne Bed Chapter 86 Question 7 of 14 View Policies Current Attempt in Progress eTextbook and Media Identify reagents that can be used to achieve the following transformation: Save for Later How To Write Biolo... O 1) NaOH, 2) RCO3H, 3) H3O+ O 1) Conc. H₂SO4, heat, 2) RCO³H, 3) H³O* O 1) Conc. H₂SO4, heat, 2) OsO4, NMO O 1) NaOEt, 2) OsO4, NMO > F1 F2 Type here to search OH OH 8- & ▶/11 a Amazon.com 150 E... F3 F4 04 F5 OH Attempts: C F6 PrtSc

Bromine reacts with alkenes in methanol according to the equation when this reaction was carried out with 4-tert-butylcyclohexene, only one isomer was formed with the molecular formula C12H23BrO (80% yield). Which of the following is the structure more reasonable for this compound? Explain your reasoning through a corresponding mechanism.

Draw the structure of the major organic product you would expect from the reaction of 1-bromopropane with Nal. You do not have to explicitly draw H atoms. • Draw only the product derived from 1-bromopropane. Do not draw other organic by-products.

f. g. OCH 3 CO₂H OCH 3 pyruvic acid 1. SOCI22 2.? NaBH4 CH3OH methicillin (narrow-spectrum, B-lactam antibiotic)? H₂SO4 (cat) C6H8O4 (show structure)

2. Analyze each reaction below for atom economy, rating it as either good or poor. Explain your answers. Reaction A (2-bromo-2-methylpropane reacts with sodium ethoxide to form methyl propene) CH3 CH3 0151016 CH3CCH3 + CH3CH,ONa Br H₂C C-CH3 + CH3CH₂OH + NaBr Reaction B (Methyl propene reacts with hydrogen bromide to form methyl bromide) CH3 H₂C=C-CH3 + HBr CH3 H3C-C-CH3 Br

What are the products of the following reactions?

2. For each of the chemical substitution reactions below identify the major products and whether the reaction is likely an SN1 or SN2. Br NACN ethanol-water CH,OH / H,0 Nal (1 equiv.) acetone CI CH;CH,OH 25°C 3. For each of the following compounds provide appropriate reactants and solvent systems to synthesize them by a substitution reaction. Show which type of substitution: Sn1 or SN2. Br NH2 Br NACN NH, аcetone CN Br OH HBr I . Il.. NASH DMSO SH

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Draw a structural formula for the major organic product of the reaction shown below. Br Ca -85 -CuLi • Consider E/Z stereochemistry of alkenes. • Do not show stereochemistry in other cases. • You do not have to explicitly draw H atoms. • Do not include organocopper or inorganic ion by-products in your answer. Sn [F ChemDoodleⓇ

Q3.     For the following reactions, predict the products, mechanism and name all the products 4.2-hexene + chlorine gas5.Halogenation of cyclohexane in the presence of light  and catalyst6.Sulfonation of Cyclobutane  with oleum 7.Addition of HBr to methylcyclopropane

Ethers can be prepared by reaction of an alkoxide or phenoxide ion with a primary alkyl halide. Draw the structure of the expected organic product of the reaction of iodomethane with the following alkoxide ion: CH3 H3C O Na You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Do not include counter-ions, e.g., Na", I, in your answer. орy вste ChemDoodle

Ethers can be prepared by reaction of an alkoxide or phenoxide ion with a primary alkyl halide. Draw the structure of the expected organic product of the reaction of 1-iodo-2-methylpropane with the following alkoxide ic + O Na You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Do not include counter-ions, e.g., Na", I", in your answer. C opy aste

Answer to this question please! Thanks !

Hi! can anyone here help me to create a schematic diagram about the experiments: " 21. Preparation of Ethyne" by Pdst Chemistry, and "Activity 10: Functional Group Tests for Hydrocarbons" by FRETZ RMT since i dont know what a schematic diagram is, and what processes/contents should be in it. thank you

For the following reactions: Draw the products and identify the type of reaction. Identify which functional groups is undergoing the reaction: state which functional group is in the starting material and what it changed to in the product. Be sure to pay attention to stereochemistry, charges, and mixtures of possible products. CH,OH H/Pt но H. OH H. OH B. CH2OH Reaction type: Starting material functional group: Product functional group:

The theoretical yield of 1-methylcyclohexene in moles(from 2-methylcyclohexanol amount of 2.239 gram).  The theoretical yield of 1-methylcyclohexene in moles is 0.01961. 1. What is the corrected actual yield(% Relative Area for 1-methylcyclohexene is 82.81%)? The theoretical yield of 1-methylcyclohexene in moles is 0.01961. 2. . What is the calculation of the %yield of 1-methylcyclohexene?

Alkenes undergo an addition reaction with borane in tetrahydrofuran (THF). For the reaction below: BH3 THF (solvent) a Draw the structure of the major organic product. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Use wedge and hash bonds ONLY when needed to show reaction stereochemistry. If the reaction produces a racemic mixture, just draw one stereoisomer. opy aste ChemDoodle

Choose reagents to convert 2-cyclohexenone to the following compounds.

Draw structural formulas for organic products A and B in the window below. CH3CH₂OH, H₂C=CHCH₂CI Mg ether H₂ H₂C=C-Mg-Cl • You do not have to consider stereochemistry. • Draw only products having the organic portion of the original alkyl halide. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate products from different steps using the → sign from the drop-down menu. ● ? Ⓡ ChemDoodle Sn [F B ↑ H₂C- -CH3 ? ChemDoodleⓇ

$ [References] H₂O + CO₂ + Nal CH₂ HỌC CHO a = Proton transfer d E1 Elimination - f SN1 Nucleophilic substitution = b = Lewis acid/base e E2 Elimination g = SN2 Nucleophilic substitution c = Electrophilic addition The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. 1. 2. Submit Answer Retry Entire Group 9 more group attempts remaining Previous Next> Save and Exit Cengage Learning Cengage Technical Support PrtScn F6 F7 1. 2. O F4 % 5 T OH you. ♫ F5 ^ 6 Y H 1₂ H₂O NaHCO3 & 7 [Review Topics] into * 8 CH₂ H₂CH₂ CH₂ I F8 K + 73°F Sunny Home 9 O F9 L ) End 0 8:14 AM □ 6/20/2022 PgDn E = P P B F10 PgUp 4x F11 F12 Ins