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2. Classify the following alkyl halides as primary, secondary, or tertiary. Which one of these options...
3. Draw and classify the following alkyl halides as methyl-, primary (1°), secondary (11°), or tertiary...
3. Draw and classify the following alkyl halides as methyl-, primary (1°), secondary (11°), or tertiary (111°) halide: 10pts -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane; -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane;
17. Classify the following alkyl halides as primary, secondary, tertiary, or none, as appropriate. 17. Clasifique...
17. Classify the following alkyl halides as primary,
secondary, tertiary, or none, as appropriate.
17. Clasifique los siguientes halogenuros de alquilo como primario, secundario, terciario o ninguno, según corresponda. no-din-an, H, CH–CH, H,C- CH CH, -CH -BrH, -CH CH, HI H,-¢-Br HIV сн. 1
Part E Indicate whether each of the alkyl halides is primary, secondary, or tertiary. Drag the...
Part E Indicate whether each of the alkyl halides is primary, secondary, or tertiary. Drag the appropriate items to their respective bins. De asemenea, ang manging CH3CHCH2CH2CH2CI CH3CH2CHCH3 CH, primary secondary tertiary
HO Regarding the following reaction: 1) a. Classify the alkyl halide as tertiary, secondary, or primary....
HO Regarding the following reaction: 1) a. Classify the alkyl halide as tertiary, secondary, or primary. b. Based on your answers to la, deduce whether the alkyl halide would be suitable for (i) only S2 reactions, (ii) only Ss 1 reactions, or (1) both/either S2 or S1 reactions. 2) a. Classify the nucleophile (the electron-sharer) as either strong or weak b. Based on your answer to 2a, deduce whether the nucleophile would be suitable for (i) only Sw2 reactions, (1)...
3. Carbocation Stability - classify the following carbocation as primary, secondary, or tertiary. highly unstable cations...
3. Carbocation Stability - classify the following carbocation as primary, secondary, or tertiary. highly unstable cations more electronegative sp2 orbital does not want to become cationic 4. Which of the following is more stable (lower in potential energy)? Explain your choice. وطرط 5. Rank the following carbocation in the order of increasing stability with 5 being the most stable carbocation. له مو و و او
Characterize the following halides as primary (1°), secondary (2°) or tertiary (3°), OR, as bonded to...
Characterize the following halides as primary (1°), secondary
(2°) or tertiary (3°), OR, as bonded to an sp2 hybridized
carbon atom (in which case 1°, 2° etc. doesn't apply)
7. (3 pts.) Characterize the following halides as primary (1°), secondary (2°) or tertiary (3°), OR, as bonded to an sp2 hybridized carbon atom (in which case 1°, 2° etc. doesn't apply) 1-bromobutane CI t-butylbromide 2-chlorobutane CI 1-chlorobutane Br Br t-butylchloride bromobenzene 2-bromobutane
3. Which one of the following alkyl halides would react faster by unimolecular nucleophilic substitution (SN.)?...
3. Which one of the following alkyl halides would react faster by unimolecular nucleophilic substitution (SN.)? PhCH,CI Phci (CH),CHCI CHCI Ph CHCI A B D E 4. Which one of the following compounds is optically active (chiral). С D A B
3. Which one of the following alkyl halides would react faster by unimolecular nucleophilic substitution (SN1)?...
3. Which one of the following alkyl halides would react faster by unimolecular nucleophilic substitution (SN1)? PhCH2C1 Phci Ph2CHCI CH3C1 (CH3)2CHCI A B С D E 4. Which one of the following compounds is optically active (chiral). A B С D E
16. Which of the following is correct regarding Sy2 reactions of alkyl halides? A. Secondary halides...
16. Which of the following is correct regarding Sy2 reactions of alkyl halides? A. Secondary halides react faster than primary halides. B. Rate of reaction depends on the concentrations of the alkyl halide only. C. Favored in polar aprotic solvents D. Results in a racemic mixture
All questions please! Classify as primary, secondary, or tertiary alcohol the compounds below: 4. b. Chassify as pri...
All questions please!
Classify as primary, secondary, or tertiary alcohol the compounds below: 4. b. Chassify as primary, a. Xoh b. ET CHOH c. cycle and 5. (4 points) Write Lewis Acid or Lewis Base beside each of the following: a. CH CH OH b. CHỊCHANH, c. FeBrz d. NH. 6.. (4 points) Consider the reaction of alcohols with hydrogen halides as written below: R-OH + H-X → R-X + H2O The reaction with tertiary alcohols only takes few minutes,...
3. Draw and classify the following alkyl halides as methyl-, primary (1°), secondary (11°), or tertiary (111°) halide: 10pts -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane; -2-chloro-3,3-dimethylhexane; -4-sec-butyl-2-chlorononane; -1-bromo-4-isopropylcyclohexane;
17. Classify the following alkyl halides as primary,
secondary, tertiary, or none, as appropriate.
17. Clasifique los siguientes halogenuros de alquilo como primario, secundario, terciario o ninguno, según corresponda. no-din-an, H, CH–CH, H,C- CH CH, -CH -BrH, -CH CH, HI H,-¢-Br HIV сн. 1
Part E Indicate whether each of the alkyl halides is primary, secondary, or tertiary. Drag the appropriate items to their respective bins. De asemenea, ang manging CH3CHCH2CH2CH2CI CH3CH2CHCH3 CH, primary secondary tertiary
HO Regarding the following reaction: 1) a. Classify the alkyl halide as tertiary, secondary, or primary. b. Based on your answers to la, deduce whether the alkyl halide would be suitable for (i) only S2 reactions, (ii) only Ss 1 reactions, or (1) both/either S2 or S1 reactions. 2) a. Classify the nucleophile (the electron-sharer) as either strong or weak b. Based on your answer to 2a, deduce whether the nucleophile would be suitable for (i) only Sw2 reactions, (1)...
3. Carbocation Stability - classify the following carbocation as primary, secondary, or tertiary. highly unstable cations more electronegative sp2 orbital does not want to become cationic 4. Which of the following is more stable (lower in potential energy)? Explain your choice. وطرط 5. Rank the following carbocation in the order of increasing stability with 5 being the most stable carbocation. له مو و و او
Characterize the following halides as primary (1°), secondary
(2°) or tertiary (3°), OR, as bonded to an sp2 hybridized
carbon atom (in which case 1°, 2° etc. doesn't apply)
7. (3 pts.) Characterize the following halides as primary (1°), secondary (2°) or tertiary (3°), OR, as bonded to an sp2 hybridized carbon atom (in which case 1°, 2° etc. doesn't apply) 1-bromobutane CI t-butylbromide 2-chlorobutane CI 1-chlorobutane Br Br t-butylchloride bromobenzene 2-bromobutane
3. Which one of the following alkyl halides would react faster by unimolecular nucleophilic substitution (SN.)? PhCH,CI Phci (CH),CHCI CHCI Ph CHCI A B D E 4. Which one of the following compounds is optically active (chiral). С D A B
3. Which one of the following alkyl halides would react faster by unimolecular nucleophilic substitution (SN1)? PhCH2C1 Phci Ph2CHCI CH3C1 (CH3)2CHCI A B С D E 4. Which one of the following compounds is optically active (chiral). A B С D E
16. Which of the following is correct regarding Sy2 reactions of alkyl halides? A. Secondary halides react faster than primary halides. B. Rate of reaction depends on the concentrations of the alkyl halide only. C. Favored in polar aprotic solvents D. Results in a racemic mixture
All questions please!
Classify as primary, secondary, or tertiary alcohol the compounds below: 4. b. Chassify as primary, a. Xoh b. ET CHOH c. cycle and 5. (4 points) Write Lewis Acid or Lewis Base beside each of the following: a. CH CH OH b. CHỊCHANH, c. FeBrz d. NH. 6.. (4 points) Consider the reaction of alcohols with hydrogen halides as written below: R-OH + H-X → R-X + H2O The reaction with tertiary alcohols only takes few minutes,...
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