What is the SN2 product when (3S,5S)-5-chloro-2,3-dimethyloctane reacts with sodium iodide and acetone.
What is the SN2 product when (3S,5S)-5-chloro-2,3-dimethyloctane reacts with sodium iodide and acetone.
Draw the skeletal structure of the major organic product of (3S,5S)-5-chloro-2,3-dimethyloctane when it reacts with sodium iodide in acetone. please use stick and wedge bonds
Draw and name the SN2 major product formed when (2R,5S)-2-bromo-5-chlorohexane is treated with sodium iodide in acetone. (Use only one equivalent of NaI.)
Draw and name the major SN2 product when (2R,5S)-2-bromo-5-chlorohexane is treated with sodium iodine in acetone. * Use only one equivalent of NaI and use wedge and dash bonds
Give the name of the product formed when 1-chloro-4-methylpentane is reacted with sodium iodide in acetone. T T T Arial 3 (12pt)
Draw the reaction equation for the Sodium Iodide/Acetone test (SN2 mechanism) for each of the substances: 1. 1-chlorobutane 2. 2-chlorobutane 3. 2-chloro-2-methylpropane 4. 1-bromobutane 5. 2-bromobutane 6. benzyl chloride 7. bromocyclohexane 8. bromocyclopentane
Select the most stable chair conformation for (1R,3S,5S)-1-chloro-3-isopropyl-5-methylcyclohexane. Select the most stable chair conformation for (1R,3S,5S)-1-chloro-3-isopropyl-5-methylcyclohexane Select the most stable chair conformation. CH(CH3)2 (1R,3S,5S)-1-chloro-3-isopropyl-5-methylcyclohexane Chair choices: CI CH CH3 CH3 (H3C)2HC CH(CH3)2 (H3C)2HC CH3 CH3 CH3 Cl CH(CH3)2 (H3C2HC (H3C)2HC
S-3-chloro-3-methylhexane reacts with an iodide anion, I-. a) Will this reaction proceed via an SN1, SN2, E1, or E2 reaction mechanism? b) What is the IUPAC name of the product(s) of this reaction? Include R and S designations if relevant. c) After the reaction has occurred, will the product solution be optically active?
3. Benzyl bromide (C4HsCH2Br) reacts rapidly with sodium iodide in acetone, and also reacts rapidly with However, bromobenzene (CAHsBr) doesn't react under either of these bns I2 gniqmo silver nitrate in ethanol, conditions. Please explain.gO o vioieV a to 2iivitorsl S Br bas wonnuwoy linsbl oeuloco eh or m poy wol i Br 3. Benzyl bromide (C4HsCH2Br) reacts rapidly with sodium iodide in acetone, and also reacts rapidly with However, bromobenzene (CAHsBr) doesn't react under either of these bns I2...
What is the major product for the following reaction trans-2-chloro-3-methylpentane reacts with 1. NaI, acetone and then 2. NaOH, EtOH and heat.
Draw the major SN2 organic product when the substrate above is treated with one equivalent of sodium iodide in acetone. Please give explanation!