You are trying to decide if there is a single reagent you can add that will make the following synthesis possible without any other major side products:xi1. ☑2. H₂OхеiDraw the missing reagent X you think will make this synthesis work in the drawing area below.If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank.Click and drag to start drawing astructure.There is no reagent that will make this synthesis work without complications.: ☐S☐

Step 1:Our aim is to find the reagent X required for the given conversion. Step 2:The given…

Answered: You are trying to decide if there is a…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter23: Addition To A Carbonyl

Section: Chapter Questions

Problem 27CTQ

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Nitesh
Your answer is partially correct. Try again. Draw an appropriate alkyl halide and a nucleophile in conjugate base form that are required to give (S)-2-Pentanol. Alkyl halide reactant: H3C Nucleophile reactant: OH Edit (S)-2-Pentanol product: H₂C OH |||I CH3 CH3 Edit Edit
b) For the following three reactions, circle the one (circle the letter A, B or C) that would go the fastest, and place a cross through the slowest. Use mechanism to explain your answer. A HSO3 H₂ H conc H2SO4 C SO3H B H2 H2 SO3H 0 S". H2 H C
You are trying to decide if there is a reagent you can add that will make the following synthesis possible: 1. ? H 2. H3O+ NH₂ OH NH2 racemic Draw the missing reagent you think will make this synthesis work in the drawing area below. If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. There is no reagent that will make this synthesis work without complications. :□ X 5
Complete the electron-pushing mechanism for the formation of the major product in the given reaction by adding any missing charges, atoms, bonds, nonbonding electrons, and curved arrows. Predict all the products of the reaction. Do not delete any pre-drawn bonds, charges, or lone pairs. If you accidentally delete a vital part of the structure, use the undo button on the lower left of the drawing canvas. Step 1: Add curved arrows. H H T H 150 °C Step 2: Draw the products, including any lone pairs. H F H H H H
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 3-bromocyclopentene from cyclopentane. Drag the appropriate items into the bins. Note that each bin should hold only one item, and not all reagents and structures will be used. Reagent 3 Reagent 2 Reagent 1 Final product Reactant Step 1 product Step 2 product (cyclopentane) (3-bromocyclopentene) NBS ROOR HBr HBr ROOR Br Br2 Br2 Hzо hv Br Br Br Br Br (CH3)3CO K
An organic chemistry Teaching Assistant (TA) suggested in your last discussion section that there is only one major organic product of the following reaction and that this reaction builds a ring. If the TA is right, draw the product in the drawing area below. If the TA is wrong, just check the box below the drawing area. NaOH ? Click and drag to start drawing a structure. The TA is wrong. ☐: อ P
4.) Propose a synthesis for the reaction given below, using only the sources of carbon listed in the reactants. You may use any other inorganic reagents needed. For each step, show the reagents used and the intermediate formed. (Note: I do not need to see any arrow-pushing, only starting materials, reagents, intermediates, and the final product) (10 points) OH + excess CH3Br
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.
Step 2 Draw the one-step synthesis for this compound using an SN2 reaction. Use Br¯ as leaving group. Add curved arrow(s) to show moving of electrons in your mechanism. Include lone pairs and formal charges in your answer. Do not show metal cation in your mechanism. CH, `CH, Edit Drawing
Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. (please show which structure I need to put as the answer).

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