Cch 2 ch 3 a b a b h 3 cch 2 nhme a b ih 2 ccbrclf a

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C–CH 2 –CH 3 A B A B H 3 C–CH 2 –NHMe A B IH 2 C–CBrClF A B H 3 C OH CH 3 3. Provide a Newman projection for the following molecules. As illustrated in the example, sight along the labeled bond from "A" to "B" unless requested otherwise. Chem 33, Kanan & Stack, 2012 PS 2; pg 2
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4. Hybridization (a) Complete the table below by indicating the approximate hybridization and approximate bond angles for the molecules illustrated. Place your answer in the appropriate box in the table. Compound Hybridization Bond Angle C N O (idealized) CO 2 HCN H 3 CNO 2 H 2 COH + N/A N/A N/A OCO = HCN = CNO = COH = (b) Provide the idealized hybridization (i.e., p, sp, sp 2 , sp 3 ) of each indicated atom in the molecules below. H CH 3 O H 3 C CH 3 CH 3 CH 3 O H 3 C H N H 3 C H 3 C CH 3 CH 3 CH 3 5. The proper naming of molecules is an essential component of learning the "language" of organic chemistry. Accordingly, please provide the appropriate line-drawing structure for each of the five molecules listed below. (a) 2-methyl-3,4-diethyl-1-hexene (b) 2,6-dimethyl-3-octyne (c) 6-butyl-1,4-cycloheptadiene dictyotene: A sex attractant produced by female gametes in marine brown algae (d) 3,7-dimethyl-2,6-octadiene-1-ol: geraniol: A fragrant, pale yellow liquid alcohol, C 9 H 17 COH, derived chiefly from the oils of geranium and citronella and used in cosmetics and flavorings.
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