(a) What is the hybridization of the carbon in the methyl cation (CH3*) and in the methyl anion (CH3¯)? (b) What is the approximate H-C-H bond angle in the methyl cation and in the methyl anion?
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- (iii) In the presence of a suitable catalyst, 2-methylpropene forms a mixture of dimers. Two of these dimers react with hydrogen to form * 2,2,4-trimethylpentane. Draw the skeletal formula for 2,2,4-trimethylpentane. Use this to draw the skeletal structure of one of the dimers formed from 2-methylpropene. 2,2,4-trimethylpentane DimerA certain hydrocarbon has a molecular formula of C5H8. Which of the following is not a structural possibility for this hydrocarbon: (d) It contains an alkyne O It contains one ring and one double bond (c) It contains two double bonds and no rings O (b) It contains one ring and no double bondsDraw the structure of a hydrocarbon with molecular formula C6H10 that also contains: (a) a carbon–carbon triple bond; (b) two carbon–carbon double bonds; (c) one ring and one C=C.
- (5c-201-5) Draw a skeleton structure and give the IUPAC name of a molecule with one alcohol group, 5 total carbons, and one methyl substituent group.True or false: (a) The C¬C bonds in benzene are all the samelength and correspond to typical single C¬C bond lengths.(b) The C¬C bond in acetylene, HCCH, is longer than theaverage C¬C bond length in benzene.Write a condensed structural formula, such as CH3CH3, and describe the molecular geometry at each carbon atom.(a) 2-propanol(b) acetone(c) dimethyl ether(d) acetic acid(e) 3-methyl-1-hexene
- 11. Which statement is true of the carbon-carbon bonds in benzene? (a) They are identical to the carbon-carbon bonds in cyclohexane. (b) They are identical to the carbon-carbon bonds in cyclohexene. (c) They are half-way between a double and single bond. (d) They are easily broken in chemical reactions. (e) They are all double bonds. ct Copyright O 2002 McGraw-Hill Ryerson Limited Name: Class:Write structures for the three isomers of the aromatic hydrocarbon xylene, C6H4(CH3)2.For the following, you must draw an appropriate structure that has the chemical formula C5H7O2Cl with the indicated functional group(s) and/or property. In each case, identify any other functional groups in the molecule you draw, that were not indicated in the question. You may use Lewis or bond- line structures to draw your molecules. You may not use the same structure to answer more than 1 question. a) An acyclic molecule that cannot form hydrogen bonds with itself b) A tertiary chloride c) A cyclic ether
- 38. Using a catalyst, two gaseous hydrocarbons, X and Y, were produced from heating hexane, C6H14. The gases were individually tested with aqueous bromine. For X, aqueous bromine became colorless, while for Y, the reddish-brown color of aqueous bromine was retained. Which of the following best describes the identity of the two hydrocarbons? (A) X= alkane, Y = alkene (B) X = alkene, Y = alkane (C) Both X and Y contain the same number of carbon atoms. (D) Both X and Y contain the same number of hydrogen atoms.For part b. Identify as an Alkane, alkene, alkyne, aromatic, alcohol, ether, aldehyde, ketone, carbocylic acid, Ester, or amine.write the structure formulas of alkanes with molecular formula C6H14, which with chlorine give: a) three monochlorinated isomers? b) five monochlorinated isomers c) only two monochlorinated isomers