Construct a three-step synthesis of 1-bromopropane from propane by dragging the appropriate formulas into the bins. Note that each bin willl hold only one item, and not all of the given reagents or structures will be used. Reactant Reagent 1 Step 1 Product Reagent 2 Step 2 Product Reagent 3 Final Product (1-bromopropane) (propane) Br2 Br2 (CH)3CO K HBr ROOR HBr NBS ROOR HaC Нас Нас, Нас Нас НаС. hv CH2 CH2 CH Нс CH-Br CH-Br CH Нас Нас, нC Нас НаС Br Br Br

Construct a three-step synthesis of 1-bromopropane from propane by dragging the appropriate formulas into the bins. Note that each bin willl hold only one item, and not all of the given reagents or structures will be used. Reactant Reagent 1 Step 1 Product Reagent 2 Step 2 Product Reagent 3 Final Product (1-bromopropane) (propane) Br2 Br2 (CH)3CO K HBr ROOR HBr NBS ROOR HaC Нас Нас, Нас Нас НаС. hv CH2 CH2 CH Нс CH-Br CH-Br CH Нас Нас, нC Нас НаС Br Br Br

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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Macmillan Learning Use the table of bond dissociation energies to calculate and compare the enthalpy of monobromination and monochlorination for the given alkyl position. Bond Dissociation Energies (for A-B- A+B) Bond broken H-H Br-Br CI-CI CH₂CH₂CH₂-H+ Br₂ CH₂CH₂CH₂-H + Cl₂ AH (kJ/mol) Bond broken AH (kJ/mol) 436 366 193 432 243 H-Br H-Cl CH₂CH₂CH₂-Br + HBr CH₂CH₂CH₂-CI+HCI Bond broken AH (kJ/mol) CH₂CH₂CH₂-H 423 CH₂CH₂CH₂-Br 294 CH₂CH₂CH₂-CI 354 AH = ΔΗ = -58 Incorrect -131 Incorrect kJ/mol kJ/mol
The following two step synthesis reduces the amount of waste generated by incorporating most of the atoms in the reagents into the products. Predict the products of each step.
Construct a three-step synthesis of trans-2-pentene from acetylene by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used. (Me methyl, CHs; Et ethyl, CH3CH2.) Reactant Product Reagent 1 Reagent 2 Step 1 Product Step 2 Product Reagent 3 (acetylene) (trans-2-pentene) Li HBr На Pt 1) NaNH2 2) Me н CH3CH2NH2 H H 1) NaNH2 2) EtBr
Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.
Identify the correct reagent/s for carrying out each of the following reactions shown below.
4) Design a complete synthesis for each of the following transformations. More than one step is required. SO3H = Br. 0=d H₂N CI NH₂ = 0= O₂N 0= OH NO₂ NO₂ سلم 'Br OH for
In the reaction series below, write down the appropriate reagents that can be used where there are question marks.
Construct a three‑step synthesis of 1,2‑epoxycyclopentane from bromocyclopentane by dragging the appropriate formulas into the bins. Note that each bin should hold only one item, and not all of the given reagents or structures will be used. Reactant −→−−−−reagent 1 →reagent 1 Step 1 product −→−−−−reagent 2 →reagent 2 Step 2 product −→−−−−reagent 3 →reagent 3 Final product
Construct a three-step synthesis of trans-2-pentene or trans-pent-2-ene from acetylene by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used. Reactant (acetylene) HC=CH HC=C-CH, Incorrect reagent1 (1) NaNH, (2) CH₂ Br HBr Step 1 product HC=C-CH,CH3 H3C. CH3 H reagent2 (1) NaNH, (2) CH₂CH₂ Br Answer Bank H₂, Pt/C Step 2 product H₂C-C=C-CH₂CH3 reagent3 Na, NH3 H Product CH3 CH3 H
Your task is to convert 2-bromobutane to 1-butene in highest yield. Which reagents would you use? O KOH/H2O O KOH/CH,OH O CH3CH2ONA/CH3CH2OH O CH3ONA/CH3OH O (CH3)3COK/(CH3)3COH
Construct a three-step synthesis of 3-bromo-3-methyl-2-butanol from 2-methyl-2-butene by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used. Final Product (3-bromo-3- methyl-2- butanol) Reactant Step 2 Product Step 1 Product (2-methyl-2- butene) Reagent 3 Reagent 1 Reagent 2 NaBr NaH HBr/NaBr РВз Br2 Br2 Br Но Br Br hv H20 Но НО Br НО Br
In an E2 mediated elimination reaction of an alkyl halide (H-X) using NaOCH3 as base, which of the following statement is not true? O The reactivity order for alkyl halides (RX) is tertiary secondary> primary. O The rate of reaction = k2 (alkyl halide] [NaOCH₂] O The reaction occurs in a single step. O The rate is independent of the leaving group.