Answered: Part 1 Identify any nucleophiles and… | bartleby

Organic Chemistry: A Guided Inquiry

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter26: Aldol And Claisen Reactions

Section: Chapter Questions

Problem 52CTQ

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Part 1
Identify any nucleophiles and electrophiles in this reaction. How will they react together?
Do all curved arrows start at an electron-rich site and point toward an electron-poor site?
Did you add non-zero charges and lone pair electrons to all appropriate atoms?
Does the overall charge and number of atoms remain consistent from step-to-step?
To bring a box back to its original status, click on the reset button in the top left corner of the drawing
window.
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I was able to do a few of these on my own, but I'm really stuck with this one. Should I be flipping the third reaction? If so, how does that help me cancel out the reactants and products on both sides? Which ones should I be multiplying?
Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. HBr • You do not have to consider stereochemistry. • Do not include anionic counter-ions, e.g., I, in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ⚫ Separate resonance structures using the → symbol from the drop-down menu. 0-> + 4 CH4 On Sn [F ? ChemDoodle
3. Drawing Reaction Mechanism Arrows For the reactions that have TWO starting materials, indicate and label which species is the nucleophile and which is the electrophile. (HINT: Look at the reactants and look at the products to see where bonds form and where bonds break! Using your pK, table and bond polarity predictions will help!) Draw curved arrows to show the movement of electrons for Bond Forming and Bond Breaking in each of the reaction steps Finally, identify and label what type of elementary step is represented for each mechanism -н Name of Elementary Step н-СI: а. Н -H Name of Elementary Step: нс-о-н b. О-н CHз н Н Name of Elementary Step Н-Сі: с O-H CH3 CНз
Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. + HCI • You do not have to consider stereochemistry. • Do not include anionic counter-ions, e.g., I, in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate resonance structures using the → symbol from the drop-down menu. H₂ H₁₂ C C HECH H₂ C H2Cl H ? ▾ n CH₂ H₁₂ C HE HC CH H₂ H2 ChemDoodle H₁₂ CH2 HC C Cl H ? ChemDoodle F n [F
For the reaction scheme below, label each reactant (identified as 'reactant 1-4') as either a nucleophile (Nu) or electrophile (E). Use the box labeled for each reactant for your answer. You only need to write Nu or E for your answer. raactant 1 Reactant 1: Reactant 2: Reactant 3: Reactant 4: H-Br: reactant 2 Br: NA Chetis reactant 3 Br: |-- O reactant 4 hp
Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. + HCI You do not have to consider stereochemistry. • Do not include anionic counter-ions, e.g., I, in your answer. • • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right Separate resonance structures using the symbol from the drop-down menu. ← - CHA ? n ChemDoodle
For the reaction below identify the reactant electrophile and the nucleophile.
Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. + HBr • You do not have to consider stereochemistry. Do not include anionic counter-ions, e.g., I', in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the + symbol from the drop-down menu.
Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. + HCI •You do not have to consider stereochemistry. Do not include anionic counter-ions, e.g., I, in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom Separate resonance structures using the → symbol from the drop-down menu. • Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. + HCI • You do not have to consider stereochemistry. • Do not include anionic counter-ions, e.g., I, in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom righ Separate resonance structures using the symbol from the drop-down menu. • - Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. + HBr • You do not have to consider stereochemistry. Do not include anionic counter-ions, e.g., I, in your answer. •…
Add curved arrows to show the forming and breaking of bonds in the reaction below. C с Ċ Add/Remove step
Draw both resonance structures of the most stable carbocation intermediate in the reaction shown + HBr • You do not have to consider stereochemistry. •Do not include anionic counter-ions, e.g., I, in your answer. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate resonance structures using the symbol from the drop-down menu. C P opy aste 000▼ [片 CH
For the reaction scheme below, label each reactant (identified as 'reactant 1-4') as either a nucleophile (Nu) or electrophile (E). Use the box labeled for each reactant for your answer. You only need to write Nu or E for your answer. H-Bri Ta -Br: reactant 1 reactant 2 reactant 3 Reactant 1: Reactant 2: Reactant 3: Reactant 4: Br: reactant 4

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