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- Mechanism Explorer: Sketch and Submission (Intermediate) Reactant посъ :0: Br Tip: Only add curved arrows in this sketcher Apply Mechanism Hint Solution 1 remaining step(s) can be solved Reaction Explorer Help (Intermediate) ProductIdentify the type of elementary step. H O coordination -CH3 O bimolecular elimination O bimolecular substitution O nucleophile elimination4. Explain why the rate of formation of 1-azidopropane is different depending on which halopropane (X = F, Cl, Br, I) is used. Explain which halopropane will react fastest? ~X X = F, Cl, Br, I NaN №3 1-azidopropane
- To answer this question, you'll need to engage with mechanism explorer. To begin work, click on the link below: Tip: Add curved arrows in this sketcher to represent the electron flows for the next mechanism step: Mechanism Explorer: Sketch and Submission (Intermediate) Reactant FOD CX ® e o Tip: Add curved arrows in this sketcher to represent the electron flows for the next mechanism step Submitted Mechanism Steps Expected Mechanism Steps (Intermediate) H₂C NH₂ H₂C Apply Mechanism Hint Solution 1 remaining step(s) can be solved Mechanism Step Reaction Explorer Help (Intermediate) Product (Intermediate) Product Sketch and Submit AboveDrag the Choices A-C into the correct order of the reaction mechanism. CH3 CH3 A. (H3C)3C- :0: fast + CH3 (H3C)3C OCCH3 H F0 H slow В. (H3C)3C- (CH3)3C + :Br: Br: CH3 CH3 С. (CН3)3С + :0: fast (CH3)3C- H A В First Step Second Step Final StepTo answer this question, you'll need to engage with Reaction Explorer. To begin work, click on the link below: Mechanism Explorer: Alcohol Reaction with HBr
- 5. Use curved arrows to depict the mechanism of the following reaction: :Ö O: 4. 2 NH₂ H-O NH₂ :0 NH, ĐH NH₂ 0: H - C XX - H HI + ✪ NH₂ H H + H NH₂ -ÖH ÖH -H₂O --H₂O c H H NH₂ — NH₂ 2:— H-N: — H H-OⒸ H H O-H -ÖH H H-OⒸ H 04 H H HAnalyze the following reaction mechanisms. How many bond forming events occur in this mechanism? OH tot t + H₂O Acetone (CH3COCH 3) Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a b с d Three Two Four One :OH O.. :OHreaction of C with OH in a different solvent has been shown to have a bimolecular slow step. Which nucleophile will react faster with OH (aq) A CH,0 15. CI CH,NH" В CH,CH, Select ALL that apply a d.
- Draw out the full reaction mechanism for this acid- base reaction: Draw the arrows to show how the electrons flow from source to sink. H H | | H-C-C- Br: H H : I H C-N. H H HThe overall reactants in Equation 8-3 are R and ucts are Nu-R and L. The carbocation (R*) that appears in the reaction mecha- nism (Equation 8-2) is the only intermediate. In the S1 mechanism shown here, (a) identify each species as an overall reactant, overall product, or intermediate, then (b) sum the steps to yield the overall reaction. :Br: + Br: 11 :I: + One reason to distinguish intermediates from overall reactants and products is to know which species in the mechanism can be isolated. W 2:47 AM K 61°F Clear 10/21/2021Draw all of the steps of the mechanism for this reaction OH 0 +CH,OH HS0 +10