Concept explainers
(a)
Interpretation: The condensed structural formula for 3-ethylhexane should be drawn.
Concept Introduction: In condensed structural formula, the organic structures of the compound are written in a line of text showing all the atoms in the molecule and omitting the vertical bonds.
(b)
Interpretation: The condensed structural formula for 2-pentene should be drawn.
Concept Introduction: In condensed structural formula, the organic structures of the compound are written in a line of text showing all the atoms in the molecule and omitting the vertical bonds.
(c)
Interpretation: The condensed structural formula for 2-hexyne should be drawn.
Concept Introduction: In condensed structural formula, the organic structures of the compound are written in a line of text showing all the atoms in the molecule and omitting the vertical bonds.
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EP BASIC CHEMISTRY-STANDALONE ACCESS
- 12.58 Draw the condensed structural or line-angle formula, if cyclic, for each of the following: (12.3) a. formaldehyde c. 3-methyl-2-hexanone d. 3,5-dimethylhexanal b. 2-chlorobutanalarrow_forward12.42 Which of the following will give a positive Tollens' test? (12.4) 1-propanol b. 2-propanol c. hexanal a.arrow_forward12.52 Draw the condensed structural or line-angle formula for the alkene, aldehyde, or ketone product of each of the following reactions: (12.4) H, heat a. ОН CH; OH b. CHз — СH — СH-CH, OH [0] ОН d. CH3-CH2-CH2-CH-CH3arrow_forward
- (12.9) Which of the following has the highest boiling point? O Both H₂S and H₂O have the same boiling point that is higher than the boiling point of H₂Se. O H₂Se O H₂O O H₂Sarrow_forwardd. CH3-CH2-C-OH 16.58 Which of the following compounds are soluble in water? (16.2, 16.5) а. СH3 — СН, — СH, —С-ОН b. CH3-C-0-CH3 ers c. CH3-CH2-CH2- ОН acid Su d. .1, 16.59 Draw the condensed structural formulas for the products from each of the following reactions: (16.2, 16.3) daim a. CH3-CH2-C-OH + H,O A b. CH3-CH,-C-OH + KOH ОН c acid H, heat с. acid "ОН + С—ОН H*, heat + HO–CH2 CH3 2 d. 16.60 Draw the condensed structural formulas for the products from each of the following reactions: (16.2, 16.3) olone odw a. CH3-C -OH + NaOH || b. CHз— С— ОН + Н2О с. ОН + КОН O=arrow_forward(12.3)Which of the following has the strongest dispersion force between its molecules? O CH3CH3 O CH3CH₂CH₂CH₂CH3 O All of these have the dispersion forces with the same strength. O CH3CH₂CH₂CH3 O CH3CH₂CH₂CH₂CH₂CH3arrow_forward
- 12:46 16.48 Give the IUPAC and common names, if any, for each of the following compounds: (16.1, 16.4) CH3 a. CH3-CH-CH2-CH2-c-OH hey C- HO- b. Cl d. CH3-CH2–CH2-C-0–CH3 CH3 C-0-CH,-CH3 e. CH3-CH – CH2 CH3 OH f. CH3 CH- CH2 -СН-С-ОНarrow_forwardQ2. Using a series of steps, show how you would synthesize N-ethylpropanamide. You are given propanal and ethanamine to begin with. You may use any other reactants or catalysts that you need. The steps should be chemical reactions with the structures of the reactants and products drawn out. (10T)arrow_forwardOrganic vs Inorganic Compounds Discussion Questions and Problems Fill in the table based on your observations: Physical/Chemical Property Organic Inorganic Melting Point (high or low) Types of Bonds (Ionic or Covalent) Odor (yes or no) Combustibility (yes or no) Soluble in Nonpolar Solvents (yes or no) Soluble in Polar Solvents (yes or no) Name the functional group (not including alkane) in the following organic structures: 1. 2. 3. 4. HO.arrow_forward
- Give the iupac name of the following: 1. 2. 3. 4. CH3 CH=CH2arrow_forwardNECTRON D OUTSTION 2 BARIC CHEMISTRY H N--H -7-H- OH 2.1 Study the compounds illustrated above and answer the questions that follow: 2.1.1 Identify the compounds labelled A, B, # D, E and F. 2.1.2 State whether the compounds illustrated are organic or inorganic compound. 2.1.3 Give the chemical formulae for compound A and D. .2. Give one compound falling in the group of alcohols. Name a compound that forms the building blocks of proteins, Give any THREE importance of compound labelled D.arrow_forward11.10 Draw the condensed structural formula for alkanes or the line- angle formula for cycloalkanes for each of the following: ommo) emo2 to zslumot IS a. propane b. hexane c. heptane d. cyclohexane onstudolay the ends leboM onsqongolaarrow_forward
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