Saved Be sure to answer all parts. Name the following compound according to substitutive IUPAC nomenclature. OH (select) (select) (select) (select) (select) (select) 6 of 11 Ins PrtSc F7 F6 F8 F10 F12 F11 F9 F5 F3 & %
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- Enters the preferred IUPAC name of the connection in Figure 29.Consider the molecule: rate the priority functional groups from highest to lowest A. Alkyl chain B. Ketone C. Carbonyl D. AnhydrideThe following names are INCORRECT. Write the most probable (systematic) IUPAC name for each and draw its structure
- Give detailed Solution with explanation needed....identify the structural formula that corresponding to the compound names. If you give correct answer all compounds I will give you upvoteCompound 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-yneAnswer the following Compounds CORRECTLY by giving the IUPAC NAME OF IT. •Label with proper notations (like hyphen, commas, periods, and grouping symbols) thank u❤️
- Give a clear explanation handwritten answer...please give detailed answer of each moleculeOrgonic 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???What is the Iupac name answers of all those questions from (d) till (h)???