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Please explain which carbonation will rearrange and why
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- Consider the following reaction. CH3CH₂CH=CHCOH HCI CH3CH₂CH CHCOH c₁ CH3CH₂CH- H 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.1-Ethoxypropane is: O CH3CH₂OCH₂CH³ Ⓒ CH³CHCH₂OCH3 O CH3CH₂CH₂CH₂CH3 O CH3CH₂CH2CH2CH₂CH3 OCH3CH₂CH₂CH₂OCH39) Draw the conformer structure, Newman projection, before elimination and the elimination product of the following reaction: Br CH3ONA H
- b) DRAW THE product of each of the following reactions? DRAW expected product stereochemistry, where NEEDED TO b) חוו H3C- Pd(OAc)2 Ag2CO3 dppe H OBn 1. B2H6, THF CH3 CH3 2. NaOH, H2O2 B 0A) C) Predict the major product of the following transformation: .CO₂Et H₂O* Heat COET C₁0H 100 B) D)Elimination occurs when (Z)-3-bromohex-3-ene is treated with NaNH2. Under the same conditions, 1-bromocyclohexeneundergoes elimination much more sluggishly. Explain why
- SN1 reactions undergo carbocation rearrangements, but E1 reactions do not because the carbocation intermediate does not last as long during the elimination process. True O FalseWhat would be the major product of the following reaction? O CH3 || C6H5C-CHCH3 + D20 A) B) C) D) E) O CD3 C6H5C-CHCH3 O CH3 1-1 C6H5C-CDCH3 O CH3 C6D5C-CDCH3 O CD3 | | C6H5C-CDCD3 OD - C6H5CDCHCH3 CH3 OD room temp. ?For each reaction, decide whether substitution or elimination (or both) is possible, andpredict the products you expect. Label the major products. chlorocyclohexane + NaOCH3 in CH3OH
- ONZ IS ON Determine which substitution mechanism occurs and draw the products, including stereochemistry. + -OCH3 DMSO Br H + CH3OH Br CH,CH, CH3Draw a reaction mechanism illustrating the transition state structure and stereochemistry of the resulting product (if any).a. (R)-2-bromobutane + -OCH3 → (SN2)b. (S)-3-bromo-3-methylhexane + methanol → (SN1)c. 2-Chloro-2-methylhekxane + -OH → (E1)Predict the stereochemical outcome of the following E2 reaction: CI CI