Question

1.
Show the curved arrow mechanism for the reaction between ethoxide and methanol to give ethanol and the methoxide ion. 1st att

2.

The carbon-metal bond in organometallic Grignard reagents exhibits significant covalent character. However, we can treat thes

3.

Show the curved arrow mechanism and both products for the reaction between methyl iodide and hydroxide. 2nd attempt See Perio

4.

Identify each reactant as a Lewis acid or a Lewis base, Part 2 (0.5 point) See Hint Draw the products that result from the fo

5.

Show the curved arrow mechanism for the reaction between the given carbocation and chloride to give 2-chloro-2-methylbutane.

6.

For the reaction below, select all the atoms in the leaving group and identify the elementary mechanistic step. 1st attempt P

7.

Draw the curved arrow notation and the resulting organic product for the heterolysis of sec-butylbromide. 1st attempt I See P

8.

Draw the products that result from the following mechanism, and identify the elementary step. Remember to include all nonzero

Show the curved arrow mechanism for the reaction between ethoxide and methanol to give ethanol and the methoxide ion. 1st attempt Jual See Periodic Table See Hint OH-Ö: Add the missing curved arrow notation.

The carbon-metal bond in organometallic Grignard reagents exhibits significant covalent character. However, we can treat these compounds as electron-rich carbanions because of the large difference in electronegativity between carbon and magnesium. These reagents are great to form carbon-carbon bonds but must be kept in an anhydrous environment to work effectively. Show the curved arrow mechanism and both products for the reaction between water and the effective carbanion resulting from benzylmagnesium bromide. Do not show the magnesium and bromide in your answer. 1st attempt Il See Periodic Table See Hint Show the curved arrows between phenylmethanide and water. COCOE

Show the curved arrow mechanism and both products for the reaction between methyl iodide and hydroxide. 2nd attempt See Periodic Table See Hint :0 H Add the missing curved arrow notation CCF

Identify each reactant as a Lewis acid or a Lewis base, Part 2 (0.5 point) See Hint Draw the products that result from the following coordination step. Be sure to include all lone pairs of electrons and formal charges.

Show the curved arrow mechanism for the reaction between the given carbocation and chloride to give 2-chloro-2-methylbutane. 2nd attempt In See Periodic Table Add the missing curved arrow notation.

For the reaction below, select all the atoms in the leaving group and identify the elementary mechanistic step. 1st attempt Part 1 (0.5 point) See Periodic Table *-your

Draw the curved arrow notation and the resulting organic product for the heterolysis of sec-butylbromide. 1st attempt I See Periodic Table See Him 0 °B Add the missing curved arrow notation.

Draw the products that result from the following mechanism, and identify the elementary step. Remember to include all nonzero formal charges and lone pairs. 1st attempt I See Periodic Table See Hint Part 1 (0.5 point) Draw the products that result from the following mechanism. Remember to include all nonzero formal charges and lone pairs

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