Please explain why or why not A B C and D can be displaced! thanks! 4. X is a potential leaving group and could be displaced by the following reaction. + X Indicate if X is displaced when a. CH CH3 161.. b. Br c. OH and d. OCOCH3
4. X is a potential leaving group and could be displaced by the following reaction. Indicate if X is displaced when a. CH2CH3 b. Br C. OH and d. OCOCH
2. X is a potential leaving group and could be displaced by the following reaction. Indicate if X is displaced when a. H, b. CI or c. NH, (justify your choice).
i need help with 2 please 1. Provide de ou treatment with aqueous base, on ase. . + oH + H₂O -OM R + oH - +he + oH 2. X is a potential leaving group and could be displaced by the following reaction Indicate if X is displaced when a H, b.CI or c. NH, (justify your choice). 3. Suggest reagents that could be used to prepare (2 methods) from an aldehyde or ketone.
I know the answer is water, but I don't know why, please explain. Thanks. #2 2. Which is the best reagent(s) for the following reaction? -OH Br А) -ОН B) NaOMe C) CH3OH D) water 4. Which is the best reaction sequence for the following tran ОН CN ANNIS
Why isn't Br replaced by OH-? Please explain in detail. The compound either A or B reacts with base to form an epoxide (C). The reaction is shown below: OH HOT Br 2-bromocyclohexanol epoxide A or B
please give me the order and explain why. thanks 10. (10 pts) Arrange the letters designating the five compounds shown below and labeled A-E in order of increasing acidity, i.e. least acidic on the far left---most acidic on the far right. A CH.-C. - E-OH B C-CH-¿-OH C CH₂-C-C-oh Br Br É Br Br CH₃-CH-(-OH & &-CH₂-C-oh Br H DLALELBSC
please explain, thanks. Consider the following mechanism. A+Br- C equilibrium step 2: C+A→ D slow overall: 2A B Determine te rate law for the overall reaction (where the overall rate constant is represented as k). rate =
Which of the following molecules possess both stereogenic carbons and is a meso compound? For the following molecule, which statement is correct Which of the following will NOT increase the rate of an SN2 reaction? 6) Which of the following molecules possess both stereogenic carbons and is a meso compound? (I mark) CH3 Br Н- -ОН Н- -ОН Br Br Н. Br -OH НС Н CH2CH3 Molecule B Molecule D Molecule A Molecule C a) Molecule A b) Molecule B...
Can someone please explain why the ordering is A>D>B>E>C I know why c is first because it's primary and why A is last because it's tertiary the most stable but the middle is hard for me to understand. Reaction coordinate 2. Rank the following carbocations in order of decreasing stability