Be sure to answer all parts. Draw a stepwise mechanism for the following reaction. Part 1 out of 4 CH3COCI Nucleophilic substitution of H for Cl: :0: ८|| CH3 ( H₂Al-H [¹] [1] LiAlH4 [2] H₂O CH3CH₂OH draw structure ... [2] draw structure ... + AIH3 + CI™
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#2
![Be sure to answer all parts.
Draw a stepwise mechanism for the following reaction.
Part 1 out of 4
CH3COCI
Nucleophilic substitution of H for Cl:
:0:
C||
CH3 l
H₂AI-H
CI
[¹]
[1] LiAlH4
[2] H₂O
CH3CH₂ OH
draw structure ...
↓
[2]
draw structure ...
+ AIH3
+ CI™](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fcf5107c7-5381-47c0-8331-391a422c2fd4%2F6e3bf520-c3dc-46dc-9738-4dc9764653e2%2Ftfpqzu_processed.png&w=3840&q=75)
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- Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C HCI / H2O `NH2 reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na", I, in your answer. • In cases where there is more than one answer, just draw one. opy aste Previous NextPredict the major product of the given reaction and then draw a reasonable mechanism for the product formation using appropriate curved arrow notation. Part 1: OH H2SO4 (aq) view structure Part 2 out of 4 H,0 H,SO4 HSO, HO finish structure . draw structure . H;O*rank these from least to most reactive in nucleophilic acyl substitution with a nucleophile I)CH3COOC2H5 II) CH3COO-Na+ III)CH3COCl IV) CH3CONH2
- Scheme 1: Reagents: (a) acetic anhydride, sulfamic acid, 60°C,30min,91%; (b) Et3SiH,I2,0-5°C,30min,82%. 1) Draw the FULL, ARROW-PUSHING MECHANISM 2) Provide a verbalization of the mechanism for your reaction mechanism 3) What is happening at each step? What atom is nucleophilic? Which atom is electrophilic? Which bonds are made? Which bonds are broken? 4) Imagine you are trying to describe the reaction mechanism and I can't see your display - how would you describe the mechanism in a way that I know, that you know, what you are talking about.Show Transcribed Text H₂, Pd/C, EtOH MeMgBr (excès) puis H3O+ Me₂CuLi, Et₂O puis H₂O+ Please draw the mechanism step by step ? ? ?Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C NH₂ HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one.
- Draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions NOC XT :: [MgX]* H3C-C-0-CH3 CH₂CH₂CH3 :0: || H3C-C-CH₂CH₂CH3 + HạC—O: [MgX]* A ketone XBe sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr HO. Br Part 1: H2O HOBR + Br HBr view structure view structure HO Part 2: H20 HBr HOBR HO view structure view structuure Br Part 3 out of 4 edit structure .. edit structure ... Next part 0.0 ↑ ↑Be sure to answer all parts. Predict the major product of the given reaction and then draw a reasonable mechanism for the product formation using appropriate curved arrow notation. Part 1 out of 4 H2SO4 (aq) draw structure .
- What alkene is needed to synthesize the following 1,2-diol using the given reagents? Be sure to answer all parts. CH3CH₂CH2 [1] OsO4 followed by NaHSO3 in H₂O: [2] CH3CO3H followed by "OH in H₂O: H OH OH CH₂CH₂CH3 draw structure... draw structure ...In the problem-solving feature below, methylcyclohexanone was seen to react at its unsubstituted c carbon. Try to write a mechanism for the same reaction at the methylsubstituted carbon atom, and explain why this regiochemistry is not observed. CH₂CH₂0- H H O CH3 Н. O CH, H. :0: + CH₂CH₂OH Draw all missing reactants, reagents, Intermediates, and/or products inside the appropriate boxes by choosing buttons from the Tools (for bonds and charges), Atoms, and Templates toolbars. CH₂b).. .. Under each potential product of this E2 elimination, write "major product," "minor product," or "not formed." Me Br H Me Me OH Me Ph Ph H Me H Et Me Me Me Ph Ph Me Me Et