In which of the following pure compounds would intermolecular hydrogen bonding be expected? (Select all that apply.) CH,CH3 CH;CH,CH2CH,CH,CH2OH O CH,NHCH3 -CH,N(CH2CH3)2 None of the Above
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a. What type(s) of intermolecular forces are expected between benzyldiethylamine molecules?
b. In which of the following pure compounds would intermolecular hydrogen bonding be expected?
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- Which compound has stronger dispersion forces, propanol or heptanol?Which has a higher boiling point? Explain using london dispersion forces, dipole dipole, or hydrogen bonding. (a) CH3CH3 or CH3CH2OH (b) CH3CH2CH2CH2CH2CH2CH3 or (CH3)3C-CH(CH3)2Rank the following molecules in order of increasing strength of intermolecular forces. CH3CH2CH3 CH3CH2CH2OH HOCH2CH2CH2OH CH3C(=O)CH3
- What type(s) of intermolecular forces must be overcome when liquid hexanol (CH3CH2CH2CH2CH2CH2OH) vaporizes?what is a hydrogen bond? a,b,c or d a)a bond between two hydrogen atoms b)a strong bond between hydrogen and some other part of a covalent compound. c)a weak to moderate strength bond between the hydrogen end of a polar molecule and the negative end of a second polar molecule. d)a very strong bond between hydrogen and carbon.What Intermolecular forces wull dominate between the mixture of water and limonene? why?
- 3. Which of the following molecules would hydrogen bond with other molecules like it? For those that do hydrogen bond, draw a diagram of two molecules using a dotted line to indicate where the hydrogen bond will occur. a. Br2 b. CH3 – O – CH3 c. CH3 – O – H d. H2O e. H2SBoth stearic acid (octadecanoic acid) and oleic acid (cis-9-octadecenoic acid) have similar molar masses (284.48 g/mol and 282.47 g/mol respectively.) However, stearic acid is a solid at room temperature, and oleic acid is a liquid a room temperature. Which of the following statements best explains this phenomenon? Select one: a. The London dispersion forces are stronger in oleic acid than stearic acid. b. The hydrogen bonding is weaker in oleic acid than stearic acid. c. The hydrogen bonding is stronger in oleic acid than stearic acid. d. The London dispersion forces are weaker in oleic acid than stearic acid.Rank the compounds in each group in order of increasing strength of intermolecular forces.
- which compound has the higher boiling point (i) (CH3)3C-C(CH3)3 or (ii) (CH3)2CH-CH2CH2-CH(CH3)2Choose from: A = intermolecular H-bonding B = London dispersion forces C = intramolecular H-bonding D = dipole-dipole interaction E = ion-dipole interaction Benzene’s solubility in water is very low (0.08 g/100 mL) but that of toluene is even lower (0.06 g/100mL). This is due to a greater extent of All carbonyl compounds with 5 carbon atoms or less are hydrophilic due to ____.Ansaid and Motrin belong to the group of drugs known as nonsteroidal anti-inflammatory drugs (NSAIDs). Both are only slightly soluble in water, but one is a little more soluble than the other. Which of the drugs has the greater solubility in water?