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- Answer the following Compounds CORRECTLY by giving the IUPAC NAME OF IT. •Label with proper notations (like hyphen, commas, periods, and grouping symbols) thank u❤️Compound 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-yneRank the following groups in order of decreasing priority. −CH=CH2, −CH3, −C≡CH, −H
- Focus only on carbon 1 For carbon 1, which group has the highest priority? a,b,c or d?why? What enantiomer is carbon 1? R or S?Give IUPAC name of the following molecule and indicate Z or E. Answer all four of themPlease identify the functional groups present in each IR. Each peak. both pictures Seperately please
- In RPLC, Compound A is more polar than compound B. In which column will compound A be more retained than compound B? A. C18 B. C8 C. Phenyl bounded column D. All of the above E. None of the aboveCompare the molecular weight of 1-propanol, ethylene glycol, and ethanethiol. Do they have similar molecular weights? What information does this give you about their IMF’s?Build a model of methylcyclohexane, and use the model to complete the following Newmanprojections of methylcyclohexane in the chair conformation: a. When the methyl group is in an axial or equatorial (circle one) position, the molecule is inits lowest potential energy conformation. b. Label one Newman projection above anti and the other gauche to describe the relationshipbetween the methyl group and C3 of the ring. c. In general, which is a lower PE conformation, anti or gauche? d. Explain how your answer to b and c provide an explanation for why it is more favorable fora large group to be in an equatorial than an axial position.