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- What is the IUPAC name for the following compound? CH₂CH₂OH CH3CH₂C=CCH₂CH3 CH3 (A) 3-methyl-4-ethyl-3-hexen-6-ol B 4-ethyl-3-methyl-3,6-hexenol 3-ethyl-4-methyl-3-hexen-1-ol 3-methyl-4-(2-hydroxyethyl)-3-hexene E 3-(2-hydroxyethyl)-3-methyl-3-hexeneGive a common name (when possible) and a systematic name for each compound. ) (h) CH3C‚CCH2OCH3Give a common name (when possible) and a systematic name for each compound.(a) CH3OCH“CH2
- Name the following organic compound: CH3 S CH CH3 CH 0 CH, CH, 3-methylsulfide-2-ethoxy butane 2-ethoxy-3-methylthio butane O 3-ethoxy-2-methylthio butane O 2-methylsulfide-3-ethoxy butane O 2-ethoxy-3-methylsulfide butaneName the following compound. CI Br O2-bromo-4-chloro-6-oxyoxane ○ 6-bromo-4-chloro-2-oxyoxane O2-bromo-4-chlorocyclohexanoate ○ 5-bromo-3-chloropentanoic acid lactone ○ 1-bromo-3-chloropentanoic acid lactoneDraw the structure of the products formed in the following reactions. a) CN H,0, H* CH3 он b) H3C- -CI + CH3 c) CH3 KMNO4, A, H,O" CH3 d) Br Mg, éther CO, H*
- Describe how 1-ethylcyclohexanol can be prepared from cyclohexane. You can use any inorganic reagents, any solvents, and any organic reagents as long as they contain no more than two carbons.7.33 a-Farnesene is a constituent of the natural wax found on apples. What is its IUPAC name, including stereochemistry? 7.34 Menthene, a hydrocarbon found in mint plants, has the systematic name 1-isopropyl-4-methylcyclohexene. Draw its structure. 7.35 Draw and name the six alkene isomers, C5H1o, including E,Z isomers. a-Famesene 8.22 Name the following alkenes, and predict the products of their reaction with (1) meta-chloroperoxybenzoic acid, (2) KMnO4 in aqueous acid, and (3) 03, followed by Zn in acetic acid: (a) (b) (a) 8.23 Draw the structures of alkenes that would yield the following alcohols on hydration (red = O). Tell in each case whether you would use hydroboration- oxidation or oxymercuration-demercuration. (b)B The the following using IUPAC rules. Select the correct answer from the list below. Br (Z)-3-bromohex-2-ene (E)-4-bromohex-2-ene (E)-3-bromohex-2-ene O(Z)-4-bromohex-2-ene
- Under certain reaction conditions, 2,3-dibromobutane reacts with two equivalents of base to give three products, each of which contains two new p bonds. Product A has two sp hybridized carbon atoms, product B has one sp hybridized carbon atom, and product C has none. What are the structures of A, B, and C?For each molecule shown (1) indicate the most acidic hydrogens. (2) Draw the major resonance structures of the anion that results from the elimination of the most acidic hydrogen. (c) S ܐ CN COOCH, CNGive the IUPAC name for each compound. Part 1 of 3 CH₂CH, H,C-C-CH_CH, CH, 1 H Part 2 of 3 X CH, H H,CCH,CH,-с-с-сH CH CH,CH, I H CH₂CH₂CH, Part 3 of 3 X H CH₂CH₂CH, H,CCH, -e-c-CH,CH, H,CCH, Й