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Concept explainers
Interpretation:
The function of the given reagent has to be identified.
Concept Introduction:
When a reagent functions as a nucleophile, substitution reaction takes place and when a reagent functions as a base, elimination reaction takes place. The first step is to determine the reagent to be strong or weak nucleophile and whether it is a strong or weak base. Basicity and nucleophilicity do not always parallel each other.
When comparing the atoms in the same row in periodic table, the basicity and nucleophilicity parallel each other. An example is,
When comparing the atoms in the same column in periodic table, the basicity and nucleophilicity do not parallel each other. An example is,
Basicity measures the charge stability on atom, while nucleophlicity measures how fast a nucleophile attacks. Basicity is a
Nucleophile (Only): This category consists of reagents that act only as strong nucleophiles and not as bases. The reagent from this category involves in substitution reaction and not elimination.
Base (Only): This category consists of reagents that act only as bases and not as nucleophiles. The reagent from this category involves in elimination reaction and not substitution.
Strong Nucleophile/Strong Base: This category consists of reagents that are strong bases and also strong nucleophiles. This includes hydroxide, alkoxide ions. Generally these reagents are used for bimolecular process.
Weak Nucleophile/Weak Base: This category consists of reagents that are weak bases and weak nucleophile. This includes reagents such as water, alcohols. Generally these reagents are used for unimolecular process.
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Chapter 10 Solutions
Organic Chemistry As a Second Language: First Semester Topics
- The number of 2sp^2 hybridized atoms in is: A. 8; B. 6; C.4; D.2; E.0;arrow_forwardThe highest boiling compound from among the following isA. 2-methylheptane; B. 3-methylheptane; C. 2,2-dimethylhexane;D. octane; E. 2,2,3-trimethylpentanearrow_forwardWhich of the following features are found in the most stable structure ofCH5NO that does not have a CO bond?w. a π bond, x. two NH bonds, y. one OH bond, z. 3 lone pairsA. w, x; B. x, y; C. y, z; D. x, y, z; E. all of them.arrow_forward
- Which one of the following functional groups is not present in thecompound shownA. amine; B. aldehyde, C. ether; D. amide. E. ketonearrow_forwardWhich of the following formulas correspond to at least one compound inwhich resonance is important?w. C2H5N x. C3H5Br; y. C3H4; z. C4H6.A. w, x, y; B. x, y, z; C. w, x, z; D. w, y, z; E. all of themarrow_forwardPredict the product(s) that are formed after each step for reactions 1-4. In each case, consider formation of any chiral center(s) and draw all expected stereoisomers. 1) OH 1) HBr (SN2) 2) NaOH, heat 3) BH3, THF 4) H2O2, NaOH 2) OH 1) SOCI 2, py 2) NaOEt 3) Br2, H₂O 3) OH 1) H2SO4 conc. 2) HBr, ROOR 3) KOtBu 4) OH 1) TsCl, py 2) NaOEt 3) 03 4) DMSarrow_forward
- Which of the following rings has the least strain in its most stableconformation?A. Cyclobutane; B. Cyclopentane; C. Cyclohexane; D. Cycloheptane;E. Cyclooctanearrow_forwardThe number of different carbon skeletons that have a main chain of 9carbons and an ethyl branch isA 3; B. 4; C. 5; D. 6; E. 7arrow_forwardQ5: Classify the following pair of molecules as constitutional isomers, enantiomers, diastereomers, the same molecule, or completely different molecules. Br O CI Br OH OH 111 Br .!!!/Br F OH and ...m Br Br OH CI Br OH ་་་་་" ། ་arrow_forward
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