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- Classify the following alkyl halides (benzylic, allylic, vinyl, aryl, 3°, 2°, 1°, methyl or a combination that best describes the molecule). CH₂CH3 CH₂CH3 -H H H H- CH₂CH3 CH3 CI CI- Br of for. CI H H blank 3 blank 4 blank 2 blank 5 blank 6 blank 1 In each blank enter a one or two character code: 1st indicate if the halide is methyl, 1°, 2°, or 3° by typing: m, 1, 2, or 3 2nd indicate if the halide is benzylic, allylic, vinyl, or aryl by typing benzylic, allylic, vinyl, or aryl Do NOT put any spaces in your answer. For example, if 2° and vinyl type: 2vinyl, if just secondary type 2 -CH₂CH3For each pair of compounds, predict which one has the higher molecular dipole moment, and explain your reasoning.(a) 1-bromopropane or cyclopropaneChoose the correct answer. Choose.. Choose... An alkyne with molecular formula C5H10 A ketone with molecular formula C4H8O A ketone with molecular formula C3H8O An alkene with molecular formula C5H8 An alkene with molecular formula C5H10 An aldehyde with molecular formula C2H40 An aldehyde with molecular formula CH4O H. A saturated hydrocarbon with molecular formula C6H14 Choose..
- Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the cyano with the ortho position in benzonitrile. CEN benzonitrile • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.State the relationship between each of the six (6) structures at the bottom of this page and the primary amine 1, (identical, enantiomer, diastereomer, structural isomer, conformational isomer, or not isomeric). Describe your reasoning clearly and succinctly. CH3 NH2 „CH3 CH, 1 CH3 CH3 CH3 NH2 H,N. 7HN CH2 CH3 H3C. CH2 CH2 CH3 NH, CH3 CH3 CH3 NH2 NH2 CH3 CH3 .CH3 CH2 ČH3 CH3 CH2From the structures below which is (a) a symmetrical ether, (b) secondary alcohol, and (c) the most acidic phenol derivative?
- What is Resonance Theory? Sate five conclusions that can be drawn from the theory. State the two main experiments that were used to establish the extra stability of the benzene molecule. What are the factors that confer Aromaticity to an organic molecule? i. State the effects of substituents on a benzene derivative towards further aromatic substitution. Based on the above suggest the various types of substituents that can be attached to Benzene. What are the various ways by which alkenes may be synthesized? i. Give two examples each of Unsymmetrical alkenes and reagents. Give two examples of reactions of alkenes that result in Anti-Markonikov’s addition productsDirection: Give what is being asked on the given organic compounds. Please be guided accordingly. NOTE: The highest score is 25 points, on the other hand, it is on the teachers' decision to give point if your answer is wrong to give way for considerations. CH₂ CH₂ CI I CH₂CH₂ NAME: CONDENSED FORMULA EXPANDED CONDENSED FORMULA: MOLECULAR FORMULA: C3 H7 b. NAME: CONDENSED FORMULA: EXPANDED CONDENSED FORMULA: MOLECULAR FORMULA: Br CHICHI CHO CH₂ CH₂write structural formulas for all the compounds that are trichloro derivatives of cyclopropane, which are chiral and which are achiral?
- Name according IUPAC rule, the following molecule (with configurations if needed). You will give the name as the following, X for the positions and no space between characters: (XE,XR,XS)-X-methyl... онThis problem is about the IUPAC (International Union of Pure and Applied Chemistry) nomenclature of organic compounds. Select the best name for the following molecule. Br F O (REI-2-bromo-4-fluorohex-3-ene O (S,Z)-2-bromo-4-fluorohex-3-ene O (R.Z)-2-bromo-4-fluorohex-3-ene O (5,D-2-bromo-4-luorohex -eneIndicate which compound in each of the following pairs has the higher value of the specified property, or if the two compounds in a pair have nearly the same value for the property. Supply the compound name or same. A: I. methyl propanoate or II. pentanal: boiling pointB: I. methyl butanoate or II. hexanal: solubility in waterC: I. methyl propanoate or II. 1-pentanol: boiling pointD: I. methyl pentanoate or II. hexanoic acid: solubility in waterE: I. butanoic acid or II. methyl propanoate: boiling point