Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the appropriate items into the bins. Note that each bin will hold only one item, and not all reagents and structures will be used. Reagent 3 Reagent 1 Reagent 2 Final product ((2-bromoethyl)benzene) Reactant Step 1 product Step 2 product (ethylbenzene) HBr NBS HBr Br2 CH3 Br. Н.С CH2 НС Br2 Br Br Br CHз CH ROOR CH2C2 ROOR hv CH2 CH Br. НС CH2 Н.с CH (CH3)3CO K*

Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the appropriate items into the bins. Note that each bin will hold only one item, and not all reagents and structures will be used. Reagent 3 Reagent 1 Reagent 2 Final product ((2-bromoethyl)benzene) Reactant Step 1 product Step 2 product (ethylbenzene) HBr NBS HBr Br2 CH3 Br. Н.С CH2 НС Br2 Br Br Br CHз CH ROOR CH2C2 ROOR hv CH2 CH Br. НС CH2 Н.с CH (CH3)3CO K*

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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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
Fill-in-the-box II ( Design a synthesis that would lead to the formation of the desired product. Fill in the boxes with the required reagents and intermediates. Students with no printer please draw a set of numbered boxes and place answer inside. Reagents Product A Reagents Reagents Product B Ph + Enantiomer
The S 1 mechanism starts with the rate-determining step which is the dissociation of the alkyl halide into a carbocation and a halide ion. The next step is the rapid reaction of the carbocation intermediate with the nucleophile; this step, completes the nucleophilic substitution stage. The step that follows the nucleophilic substitution is a fast acid-base reaction. The nucleophile now acts as a base to remove the proton from the oxonium ion from the previous step, to give the observed product. Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all nonzero formal charges. Draw or edit atoms, groups, or bonds Add/Remove step 2 9 Click and drag to start drawing a structure. ale
lost on this guy as well Be sure to answer all parts. Determine a stepwise mechanism for the following reaction that illustrates why two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a wide ph Meme under Sx1 reaction conditions, even though it is a 1° alkyl halide. 1-bromohex-2-ene CH₂OH Part 1: The first step in the reaction proceeds according to which mechanism? CH₂CH₂CH₂CH=CHCH₂ CH₂CH₂CH₂CH=CHCH₂ + CH₂OH Part 2 out of 5 Draw the missing resonance contributor. Check my work OCH₁ CH₂CH₂CH₂CH=CH-CH₂ + Br CH₂CH₂CH₂CH=CHCH₂ CH OCH₂ edit structure... Next part +HBr
Draw the products of the three step reaction sequence shown below. Ignore inorganic byproducts. If the reaction results in a mixture of ortho and para isomers, draw only the para- product. Select to Draw 1. KCN, THE 2. H3O*, heat Select to Draw CH3CH2C(O)CI (1 equiv) AICI3 NBS hv Select to Draw NH2NH2, KOH heat Select to Draw
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show all steps and use the arrows correctly. Propose a mechanism that explains the product for the following reaction. Be sure to ILO H₂SO, OH Xo
Draw the major organic product(s) of the following reaction. Br + NaCN DMF • You do not have to consider stereochemistry. • If no reaction occurs, draw the organic starting material. • When SN1 & E1 pathways compete, show both the substitution and the elimination products. Separate multiple products using the + sign from the drop-down menu. .Do not include counter-ions, e.g., Na+, I, in your answer. ? n ChemDoodle
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Answer all parts of all the questions
5. Complete this sequence of reactions. Provide a mechanism for each step along the way. 1) CH₂MgBr 2) H₂O+ ? 1) NaH 2) CH₂CH₂Br