Concept explainers
(a)
Interpretation: The structures for the major products of the given reactions are to be drawn.
Concept introduction: When reagents such as
To determine: The structure for the major product of the given reaction.
(b)
Interpretation: The structures for the major products of the given reactions are to be drawn.
Concept introduction: When reagents such as
To determine: The structure for the major product of the given reaction.
(c)
Interpretation: The structures for the major products of the given reactions are to be drawn.
Concept introduction: When reagents such as
To determine: The structure for the major product of the given reaction.
(d)
Interpretation: The structures for the major products of the given reactions are to be drawn.
Concept introduction: When reagents such as
To determine: The structure for the major product of the given reaction.
(e)
Interpretation: The structures for the major products of the given reactions are to be drawn.
Concept introduction: When reagents such as
To determine: The structure for the major product of the given reaction.
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Chapter 22 Solutions
Bundle: Chemistry, Loose-Leaf Version, 10th + OWLv2, 4 terms (24 months) Printed Access Card
- Alcohols are very useful starting materials for the production of many different compounds. The following conversions, starting with 1-butanol, can be carried out in two or more steps. Show the steps (reactants/catalysts) you would follow to carry out the conversions, drawing the formula for the organic product in each step. For each step, a major product must be produced. (See Exercise 62.) (Hint: In the presence of H+, an alcohol is converted into an alkene and water. This is the exact reverse of the reaction of adding water to an alkene to form an alcohol.) a. 1-butanol butane b. 1-butanol 2-butanonearrow_forwardtype of organic reactionarrow_forward1. Dehydration: 2. Oxidation: This is a reaction where an alcohol loses a water molecule to form an alkene. For example, when ethanol is treated with an acidic catalyst, such as sulfuric acid, it undergoes dehydration to form ethene (CH2=CH2) and water. ALCOHOLS In this reaction, an alcohol is converted to either a carbonyl compound or a carboxylic acid. 3. Esterification: Types of Reaction (s) For example, primary alcohols can be oxidized to aldehydes or carboxylic acids, while secondary alcohols can be oxidized to ketones. Tertiary alcohols are usually not affected by oxidations 4. Substitution: The conversion of an alcohol and a carboxylic acid to an ester and water, in the presence of an acid catalyst. The reaction between methanol and acetic acid to form methyl acetate: CH3OH + CH3COOH CH3COOCH3 + H2O Click to add speaker notes ME Substitution reactions in organic chemistry involve the replacement of one atom or group of atoms with another atom or group of atoms in a molecule. 1.…arrow_forward
- For the following reaction, draw the major organic product and select the correct IUPAC name for the organic reactant. If there is more than one major product, both may be drawn in the same box. When drawing hydrogen atoms on a carbon atom, either include all hydrogen atoms or none on that carbon atom, or your structure may be marked incorrect. H. HBr Select the correct IUPAC name for the organic reactant: 2-methylbutene 2-methyl-3-butene 4-methyl-1-pentene 3-methyl-1-butenearrow_forwardOrganic compounds are classified into chemical families on the basis of similarities in chemical properties; these similarities are primarily due to the presence of characteristic arrangements of atoms known as ___.arrow_forwardHow does the structure of an alcohol differ from an ether? Describe how an aldehyde differs in structure from a ketone. Thiols are compounds which resemble alcohols, except that the oxygen atom is replaced by a sulfur atom. Draw the analogous thiol for the four carbon alcohol in Table 1. Describe the structural difference between carboxylic acids and esters. Are ethers polar molecules? Would you expect ethers to have higher or lower boiling points than alkanes (circle one)? Explain. Pentane (an alkane) has a boiling point of 36 °C. Does the data agree with your prediction? explain why this could be the casearrow_forward
- Identify the following organic reactions whether it is addition, elimination, substitution, or rearrangement. Write your answers in CAPITAL LETTERS. 1. CH;CH=CH2 H2 CH;CH2CH3 2. CH3CH,Br LIOH CH3CH2OH LiBr 3. CH3CH,CH2CI CH;CH=CH2 + HCI HO H,SO, 4. + H20 Br 5. Br, Br OH H,SO, H CI 7. H-C-CI + Cl-CI → H-C-CI H-CI Cl H H H. 8. H - C H H H OH H. H H H H 9. + HX H -C C-X H Br OH H2O 10. + HBr 6.arrow_forward- Identify each organic compound as an alkane, alkene, alkyne, aromatic hydrocarbon, alcohol, ether, aldehyde, ketone, carboxylic acid, ester, or amine, and provide a name for the compound. H CH,-CH-N-CH,-CH,-CH,-CH, CH3arrow_forwardOrganic compounds may have characteristic odors as well as other characteristic physical properties. For example, the distinct odor of the seashore at low tide results in part from the presence of dimethyl sulfide (CH3SCH3), a molecule with a similar structure to dimethyl ether (CH3OCH3). Ethanethiol (CH3CH2SH), also called mercaptan, is an isomer of dimethyl sulfide with a much less pleasant odor.The table lists four related compounds and their enthalpies of vaporization (ΔH°vap) in kJ/mol. Compound ΔH°vap (kJ/mol) CH3OCH3 23 CH3SCH3 28 CH3CH2SH 27.5 CH3CH2OH 42 Rank the following compounds in order of increasing strength of their intermolecular forces, given the ΔH°vap listed for each. Place the compound with the strongest intermolecular forces (IMFs) at the top of the list. (Strongest to weaknest). Why is ΔHºvap for CH3SCH3 greater than ΔHºvap for CH3OCH3? A. CH3OCH3 is more polar. B. CH3SCH3 has stronger dipole–dipole attractions. C. CH3OCH3 can form…arrow_forward
- 16. An atom or group of atoms that can give organic compounds distinct chemical and physical properties. 21. When a compound with the general formula R-COOH loses a proton, the product that remains is described with this term. Its general formula is R-COO- 24. A class of organic compounds in which three or more carbons form a ring structure. All of the carbon-to-carbon bonds are single bonds in this family of compounds.arrow_forwardComplete the organic reaction.arrow_forwardBoth aldehydes and ketones contain carbonyl groups. In aldehydes, the carbonyl carbon atom is bonded to a hydrogen atom, whereas in ketones, the carbonyl carbon atom is bonded to another carbon atom. Select the true statements about aldehydes and ketones. - Ketones have lower boiling points than alcohols of similar size. - Aldehydes contain a carbon–oxygen double bond. - Butanal has a higher boiling point than 2-butanol. - Aldehydes with more than five carbon atoms are soluble in water, but not organic solvents. - Both aldehydes and ketones can hydrogen bond with water molecules. - Propanal is a gas at room temperature, whereas formaldehyde (methanal) is a liquid at room temperature.arrow_forward
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