Rank the following carbonyl containing compounds from the least stable (bottom) to the most stable (top). Drag and drop options into correct order and submit. For keyboard navigation... SHOW MORE 요요 11 H H
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Q: d. с. b. НО ОН Н. H₂SO4 я Н ed o CH₂N2 Д NaOCH3 СН3ОН, Д are 108 H sa SID:
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- Orgonic Chemistry II: The answer is writtten as followed. But I Need Explanation. My question is that: Can I siwtch reagent 2 to reagent 1? for example reagent 1 is Cl2,Fecl3, can I changed it to reagent 2??? Why and why not???In depth explanation of each, please.What is the correct answer here? Answer key says D but it doesn't make sense to me because the final one (5) is tertiary allylic.
- Do all that's asked please label so I knowCompound X is insoluble in cold KMnO4, Br2 in CCl4, and conc. H2SO4. Compound X is most likely: a. an alkane b. none of these c. an alkene d. an alcohol e. an alkyl halide Indicate which of the ff. statements regarding nucleophilicity is incorrect. F- is more nucleophilic, hence, more reactive towards methyl iodide than Cl-. Second row elements are more nucleophilic than first row elements of comparable basicity. The rate of SN2 reaction may be markedly affected by the nucleophilicity of the attacking atom. Nucleophilicity is the affinity of a nucleophile to an electrophilic carbon Which of the following alkynes can be deprotonated by NaNH2 in liquid NH3? 3-Methylhex-2-yne Pent-2-yne 3-Methylbutyne none of these Hex-3-ynei need help filling out the following SN2 reactions with appopiate reactants, products, or reagents,
- What is the Iupac name answers of all those questions from (d) till (h)???Assign the stereochemical configuration (E or Z) for the alkene below. Show your work, indicating clearly which groups are assigned high priority (e.g., through assigning the groups numbers, circling only the high priority groups, or labeling groups as high or low).All attempts to isolate primary and secondary nitroso compounds result solely in the formation of oximes. Tertiary nitroso compounds, however, are stable. Explain.
- For SN1 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure to explain if alkyl halides did not react or did react and why. 3o (tertiary) compounds listed are: 2-chloro-2-methylpropane (see picture) Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature.#6). Second picture shows instructions on how the arrows must be shown as.You react an unknown aldehyde (substitutent group marked with an "x") with a ketone and get the product on the right (substitutent group still unknown). HNMR data for the product is shown below. Which of these 3 aldehydes is the reactant that was used? sorry the HNMR looks rough, this was the last question on my final and I am still kinda reeling from it.