Identify the a and ß carbons in the alkyl halide. The a carbon(s) include: 0 10...
Be sure to answer all parts. Part 1: Identify the a and ß carbons in the alkyl halide. 2 1 Br The a carbon(s) include: 0 1 0 2 0 3 0 4 The ß carbon(s) include: 0 10 20 30 4 Part 2 out of 2 Draw the possible elimination products formed when the alkyl halide is treated with K+ COC(CH3)3. Elimination product formed when carbon 1 is the ß carbon: draw structure ... Elimination product formed when carbon...
1. Draw the structure of any secondary alkyl halide containing at least six carbons. 2. Name it. 3. Circle the alpha carbon. 4. Draw box around all the beta carbons. 5. Draw the product(s) for the elimination reaction product for your choosen alkyl halide.
Draw the possible elimination products formed when the alkyl halide is treated with K-OC(CH). Elimination product formed when carbon 1 is the ß carbon: draw structure ... Elimination product formed when carbon 2 or 4 is the ß carbon: draw structure...
How would you carry out the synthesis below? Additional
carbons may come from any alkyl halide with 3 C's or less. Show the
reagents needed for each step of your transformation, but do NOT
draw the mechanisms for each step.
SHORT ANSWER #30: How would you carry out the synthesis below. Additional carbons may come from any alkyl halide with 3 C's or less. Show the reagents needed for each step of your transformation, but do NOT draw the mechanisms...
Identify the alkyl halide that generates ethanol. e alkyl halide that generates the most stable carbocation in aqueous a. bromoethane b. bromomethane c. 2-bromo-2-methylpropane d. 2-bromopropane
please answer for me all questions 1-20
1) Identify the alkyl halide that reacts the fastest in a Sn2 reaction. A) chloromethane B) 2-chloro-2-methylpropane C) 2-chlorobutane D) 1-chlorobutane 2) Identify the alkyl halide that reacts the fastest in an SN 2 reaction. A) 1-bromopropane B) 1-fluoropropane C) 1-chloropropane D) 1-iodopropane 3) Which of the following alkyl halides gives the slowest SN2 reaction? A) CH3CH2C1 B) Ci CH3CCH2CH3 CH3 C) CH3CHCH2CH3 CH2 CH3CHCHCH3 C1 СН3 4) Which of the following alkyl...
Categorise this alkyl halide as primary / secondary / tertiary, and identify the most electrophilic (8+) location within the molecule. a Br е Select one: Secondary alkyl halide; the electrophilic location is b Secondary alkyl halide; the electrophilic location is a Tertiary alkyl halide; the electrophilic location is a Primary alkyl halide; the electrophilic location is a 0 Tertiary alkyl halide; the electrophilic location is e
How would you carry out the synthesis below? Additional carbons may come from any alkyl halide with 30's or less, Show the reagents needed for each step of your transformation, but do not draw mechanisms for each step. the -->
1. Label the a carbon and ß-carbons in each of the following compounds, 2. Determine the (E) and (Z) configuration and give the IUPAC name for the following alkenes.
R-x 1. Prepare the following compounds from any simple alkyl halide having four carbons or less (can be branched, but no other functional groups), ethylene oxide, cyclohexane, and/or cyclopentane. Any other carbon-containing reactants must be synthesized from the above mentioned reagents! Show all steps and reagents.