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- The reaction below is a base-catalyzed aldol reaction. O || CH₂-C-H CH3-C-H Ethanal (Acetaldehyde) H I CH3-C-H Ethanal (Acetaldehyde) NaOH Draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions AC⇒x= :O: || :CH₂-C-H OH Bl CH3-CH—CH2-CH -CH₂-1-1 a 3-Hydroxybutanal (B-hydroxyaldehyde; formed as a racemic mixture) :0: :0: || CH3—CH—CH2-C-H A tetrahedral carbonyl addition intermediate XO || CH3-CO-C-CH3 tCH3CH2CH, NH CH 3 | CH3-C-CL + CH3-N-CH3 Complete the following reaction.use curly arrows for the mechanism of the reaction. see sample attached as a guide for the format (arrows, dots).
- Do not give handwriting solution.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 XDraw a representation of the transition state for the following endergonic mechanistic step. H;C-CH=CH, H-OH2 H3C-CH-CH; H,0
- Draw a representation of the transition state for the following endergonic mechanistic step. H,C-CH=CH, H-OH, H3C–CH-CH3 H,0The given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Reduction Rearrangement reaction Acid O || R₁-C-O-R₂ Meeting in "General"#2 - Draw the step-by-step mechanism for each of the steps in the following reaction sequence. Be sure to draw arrows for the movement of all electrons. Show any and all intermediates. ОН CH–C=C-CH2CH3 (1) Na* -:C=C-CH;CH3 NaNH, H-C=C-CH;CH3 (2) H;O+
- Draw the curved arrows for the following mechanisms. Describe what is hap step (mechanism patterns). (Take it one step at a time and note the differences). :0: R CI: H-O-H :Ö:0 :0: :CI: :CI: H2O OH OH2 Br Br H-Br O-H H-8-H :0: OH Br 1 Br H2O H₂O-CH3 HBr -Br =CH₂ CH3 Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions NA :Br: ► ×™ -CH3 -CH3 C-CH3 H4
