When (S)-3-bromopent-1-ene is heated in water, which of the following compounds is not produced? (E)-pent-2-en-1-ol pent-4-en-1-ol O(S)-pent-1-en-3-ol O(R)-pent-1-en-3-ol (Z)-pent-2-en-1-ol show work. don't give Ai and copied answer
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- 6Elimination occurs when (Z)-3-bromohex-3-ene is treated with NaNH2. Under the same conditions, 1-bromocyclohexeneundergoes elimination much more sluggishly. Explain whyWhich of the compounds below cannot be oxidized by pyridinium chlorochromate? (R)-2,3-dimethylhexan-2-ol (1R,2S)-2-methylcyclopentanol (S)-3,3-dimethylhexan-2-ol 2,2-dimethylhexan-1-ol
- Draw the product of this reaction and states its IUPAC name, and states what type of mechanism is occuring (eg. SN1, SN2, E1, E2, etc)?Predict the stereochemical outcome of the following E2 reaction: CI CIWhen (ft)-6-bromo-2,6-dimethylnonane is dissolved in CH3OH, nucleophilic substitution yields an optically inactive solution. When the isomeric halide (fl)-2-bromo-2,5- dimethylnonane is dissolved in CH3OH under the same conditions, nucleophilic substitution forms an optically active solution. Draw the products formed in each reaction, and explain why the difference in optical activity is observed.
- When (S)-1-bromo-1-phenylethane undergoes an SN2 reaction with methanethiol (CH3SH), the product of the reaction is the compound shown below. What will its configuration be? O S only R only O both R and S with slightly more S than R O both R and S with slightly more R than SDraw the major product formed for each reaction. Assume the reactions are irreversible. Include stereochemistry when products contain stereocenter(s). (d) (e) Br NaOCH3 HO CI NaHNone