
Concept explainers
Assume that an aqueous solution of a cation, represented as a blue sphere, is allowed to mix with a solution of an anion, represented as a red sphere, and that the following result is obtained:
Which combinations of cation and anion, chosen from the following lists, are compatible with the observed results? Explain.

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Chapter 7 Solutions
General Chemistry: Atoms First
- Draw the structures for each of the intermediates in the boxes provided for the synthesis below. OCH3 Fe HO HNO (CHOO pynding H₂504 LHNO2 NACH-I Fa H₂O HCL HNO 180arrow_forwardProvide structure(s) for the starting material(s), reagent(s) or the major organic product(s) of each of the following reactions or sequences of reactions. Show all relevant stereochemistry [three only] A. o 11 (CH3)CH — C— C ether (CH3)2CH-C-O-C-CH3 B. CH3 CHy CI Staf OH C. HC OCHS + H₂Oarrow_forwardConsider the reaction sequence below to answer the following questions: EtO Compound X 1. NaOEt, EtOH OEt Br CO₂Et NaOEt, EtOH Compound Z CO₂Et Compound Y A. Compound X, diethyl propanedioate, is more commonly known as a. ethyl acetoacetate b. acetoacetic ester C. oxalic ester d. malonic ester 3. Write the complete stepwise mechanism for the conversion of Compound X into Compound Y. Show all electron flow with arrows and draw all intermediate structures.arrow_forward
- Classify each of the following nitrogen atoms in the following compounds as primary, secondary, tertiary, or quaternary [three only] CH3 HO-CHCHNHCH3 A. B. C. H&C CH3 D. HO phedrine CH2CHCH3 amphetamine NH₂ mepiquat chloride faxofenadine OH H&C CH CO₂Harrow_forwardDraw the structure of the aldol self-condensation product for each of the following compounds. If a compound does not undergo aldol self-condensation, explain why it does not. A. B. CHICHCH₂OH CH3CHCH2CH CH3 CH3 C. CH 30 H3C-C-C-H CH3 questionsarrow_forward. A.Propose a synthesis for propylbenzene which avoids the problems of direct Friedel-Crafts alkylation. B. Consider the reaction below to answer the following questions. A B C NO2 Febr Brz D The Lewis acid catalyst in the reaction is: a. The nucleophile in the reaction is: b. C. d. This reaction proceeds Draw the structure of product D. (faster or slower) than benzene.arrow_forward
- Consider the reaction below to answer the following questions. HOCH CHOH На A B C D H₂Oarrow_forwardConsider the structures below to answer the following questions. A. Indicate the most acidic hydrogens in each of the molecules. OH CH-H CH₂C-H H&C མིངྒཱའི B. Rank the molecules above in order of increasing acidity (least acidic to most acidic). a. III, II, I b. II, III, I C. I, II, III d. II, I, IIIarrow_forwardConsider the reaction below to answer the following questions. H H+ A B CH₂OH 5% NaOCH, CH₂OH A. Which carbonyl compound functions as the electrophile in this reaction? B. Draw the structure of the enolate ion that is generated during the course of this reaction. C. This reaction is an example of: a. a mixed Claisen condensation. b. C. d. a Dieckman condensation. a Michael reaction. a mixed aldol reaction.arrow_forward
- Give the major organic product(s) of each of the following reactions or sequences of reactions. Show all relevant stereochemistry. [two only] CH3O (11 HC-C-C-CH3 A. CH3 12. NaOHarrow_forwardDiethyl malonate can be prepared by the following reaction sequence. Draw the structures of each of the missing intermediates in the boxes provided. 17 1. Br PBr H&C OH 2 H₂O CH3CH₂OH На NaCN H₂SO4 NC. CH CH₂OH на H₂O, heat CH₂ OCHCH3 ཝསི། ཡིཀྑཱམུདྡྷནྟ CH₂ OEtarrow_forwardThe reaction of a carboxylic acid with an alcohol in the presence of acid is termed Fischer esterification. OH + CH₂OH На B C A. The nucleophile in this reaction is B. Compound C functions as a. a base scavenger b. a solvent C. a catalyst d. a neutralizer C. Fischer esterification is an example of: . a. nucleophilic acyl addition b. nucleophilic acyl substitution c. nucleophilic acyl elimination d. nucleophilic acyl rearrangement in this reaction.arrow_forwardarrow_back_iosSEE MORE QUESTIONSarrow_forward_ios
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