1.
2.
3.
4.
5.
6.
7.
8.
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
Below is the Sn2 reaction between iodomethane and cyanide (CN). Draw the missing curved arrow notation. Add lone pairs of electrons and nonzero formal charges. ✓ 1st attempt W See Periodic Table D See Hint Nec H—• — N=C—¢-H 10 i Draw the missing curved arrow notation. Add lone pairs of electrons and nonzero formal charges.
Below is the E1 reaction between t-butyl chloride and water (H20). Draw the missing curved arrow notation in the first and second boxes to reflect electron movements. In all boxes, add lone pairs of electrons and nonzero formal charges. 1st attempt hd See Periodic Table Q See Hint CI CI CI Draw the missing curved arrow notation. Add lone pairs of electrons and nonzero formal charges.
Below is the Sn1 reaction between bromocyclohexane and iodide (1). Draw the missing curved arrow notation in the first and second boxes to reflect electron movements. In all boxes, add lone pairs of electrons and nonzero formal charges. 2nd attempt See Periodic Table See Hint Draw in the missing curved arrow notation. Add 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...
07 Question (3 points) Below is the E1 reaction between t-butyl chloride and water (H20). Draw the missing curved arrow notation in the first and second boxes to reflect electron movements. In all boxes, add lone pairs of electrons and nonzero formal charges. 1st attempt See Periodic Table See Hint HAKA Draw the missing curved arrow notation. Add lone pairs of electrons and nonzero formal charges.
Draw the missing curved arrow notation for the bimolecular elimination (E2) step shown below. Include all lone pairs and nonzero formal charges. V 1st attempt . See Periodic Table D See Hint Draw the missing curved arrow notation for the bimolecular elimination (E2) step shown below.
Peroxyacids (RCO3H) can convert alkenes into epoxides. Draw the two products and the mechanism arrows for the following reaction. Be sure to include lone pairs of electrons and nonzero formal charges on all species. 1st attempt See Periodic Table See Hint Draw curved arrow notation to show the reaction between the peroxy acid and the alkene.
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....
02 Question (2 points) Draw a mechanism for the reaction of the ketone with hydronium ion. In the first box, draw any necessary curved arrows. Show the products of the reaction in the second box. Include any nonzero formal charges and all lone pairs of electrons. V 1st attempt See Periodic Table See Hint ISO i Draw any necessary curved arrows to show the reaction between the ketone and hydronium ion.