Write the mechanism for the acetylation of vanillin in an acidic medium. Use curved arrow notation and be sure to include any non-bonding (lone pairs) of electrons, when relevant. The product is supposed to be C14H16O7
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For the reagents below, draw the major organic product of the
bimolecular substitution and use curved-arrow notation to draw the
mechanism. Be sure to draw any non-bonding electrons.
For the reagents below. draw the major organic product of the bimolecular substitution and use curved arrow notation to draw the mechanism. Be to draw any non-bonding electrons. Draw curved arrow(s) Draw product DMSO Na
NaBH4, ETOH olyto bom. Of= (stereochemistry intentionally omitted) (optically active) A. Draw a mechanism using curved arrow notation for the formation of the product in the reaction above. Make sure to include all relevant lone pairs, bonds, and formal charges. (8 pts)
Draw the expected product of the following curved arrow
mechanism. Be sure to draw a charge and the non-bonding electron
pairs.
Draw the expected product of the following curved arrow mechanism. Be sure to draw a charge and the non- bonding electron pairs 근
6. What is the correct product for the following reaction? NaOCH3 OCH3 CH3OH Hyco A: O B: O C: D: О COCH3 CO2CH3 CO2CH3 CO2CH3 7. Provide a mechanism for the reaction in problem (6). Be sure to use the correct arrow notation and include relevant lone pairs and formal charges.
6. What is the correct product for the following reaction? NaOCH3 OCH3 CH3OH Hyco A: O B: O C: D: О COCH3 CO2CH3 CO2CH3 CO2CH3 7. Provide a mechanism...
Below is the SN1 reaction of
(S)-2-iodopentane and bromide (Br–). Complete
the mechanism by providing the missing curved arrow notation, lone
pairs of electrons, and nonzero formal charges. Be sure to draw the
two organic products that will be produced in the third box.
16 Question (3 points) @ See page 407 Below is the Sn1 reaction of (9)-2-iodopentane and bromide (Br). Complete the mechanism by providing the missing curved arrow notation, lone pairs of electrons, and nonzero formal charges....
Below is the Swi reaction of (99-2-bromobutane and iodide (1) Complete the mechanism by providing the missing curved arrow notation, lone pairs of electrons, and nonzero formal charges. Be sure to draw the two organic products that will be produced in the third box 1st attempt Il See Periodic Table Please draw all four bonds at chiral centers. B 10 Draw the missing curved arrow notation. Add lone pairs of electrons and nonzero formal char
Below is the SN1 reaction of
(S)-2-iodopentane and bromide (Br–). Complete
the mechanism by providing the missing curved arrow notation, lone
pairs of electrons, and nonzero formal charges. Be sure to draw the
two organic products that will be produced in the third
box.
Below is the SN1 reaction of (S)-2-iodopentane and bromide (Br). Complete the mechanism by providing the missing curved arrow notation, lone pairs of electrons, and nonzero formal charges. Be sure to draw the two organic products...
the mechanism, using a curved arrow, include all the
lone pairs, non zero formal charges, countercharges, and
reversibility or irreversibility.
w the mechanism of the following reaction, using the curved-arrow notation to indicate the ganization of electron density. Denote all intermediates, lone pairs, nonzero formal charge mtercharges, and reversibility or irreversibility HỌC CH | HCCH excess EtOH H₃C OEt Eto .. H
16. [10 pts) Use curved-arrow notation to write out a detailed, step-wise mechanism for the following transformation. Be sure to (a) include all of your lone pairs, (b) include all formal charges, (c) draw your arrows neatly and precisely, and (d) enclose intermediates within square brackets. (If you get stuck, number the atoms of your reactant and the corresponding atoms in your product to help recognize what bonds are made and broken!)
5. [5 pts] Use curved-arrow notation to write out a detailed, step-wise mechanism for the reaction listed below. Be sure to (a) include all of your lone pairs, (b) include all formal charges, (c) draw your arrows neatly and precisely, and (d) enclose intermediates within square brackets. If you get stuck, number the atoms of your reactant and the corresponding atoms in your product to help recognize what bonds are made and broken! HBr r Mechanism: +4 +