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D.24.
![Please teach me the plausible synthesis for this transformation. Thank you!
O=S=O
I
OH
Br](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Ff7373726-0d35-46ca-aa27-97bcf9126f3a%2Fe9d3a3c5-47f7-48e9-b3fe-6190e0407661%2Fh5ev774_processed.jpeg&w=3840&q=75)
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- Formulate the reaction. Explain the stereochemistry of the products based on the mechanism of the reactions. H2SO4 Et!! Me 'Et ELOH HWhat is the predicted product for the reaction sequence shown? CH₂CH₂OH PCC 1 N IV N. LOH = (CH3)2NH H₂SO4 N V N N |||What is the relationship between the products formed in the SN1 reaction below? Options: Structural isomers Enantiomers Diastereomers Identical
- PQ-6. What is the rate determining step of this reaction? CH₂CH3 (A) HOTS H3C (C) NC CH₂CH3 HOTS H3C CH₂CH3 NaCN Hi H3C (S)-isomer (B) OTS acetone Hi H₂C (D) NC CH₂CH3 CO-H Ts CH₂CH3 ∙H H H₂C CO CN H H3C CH₂CH₂ (R)-isomer4) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors, the regiochemistry that results in each case. ỌMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3Your task is to convert 2-bromobutane to 1-butene in highest yield. Which reagents would you use? O KOH/H2O O KOH/CH,OH O CH3CH2ONA/CH3CH2OH O CH3ONA/CH3OH O (CH3)3COK/(CH3)3COH
- Do not give handwriting solution.CH3 O O CH3CH₂CHCH₂CH=CHCOH HCI CH3 CHOMO CH3CH₂CHCH₂CH- CHCOH ChemDoodleⓇ CI H CH3 CH3CH₂CHCH₂CH- O CHCOH H CI this product is not observed Account for the fact that this reaction yields only a single product by drawing the carbocation intermediate leading to the observed product. Sty √n [Fepi-Artistolochene, a hydrocarbon found in both pepper and tabacco, is biologically synthesized by the follwing pathway. Add curved arrows to show the mechanism of each step
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