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HO Regarding the following reaction: 1) a. Classify the alkyl halide as tertiary, secondary, or primary....
Please fill out the following table, indicating the category of reaction (Swi or Sm2) that will...
Please fill out the following table, indicating the category of reaction (Swi or Sm2) that will occur in each set of alkyl halides and nucleophiles. If no reaction occurs, write 'NR." Alkyl Halide Strong Nucleophile Weak Nucleophile SN2 SNZ SN2 SNI SNL SNU SNI SNI Methyl 10 2° 3° When determining which mechanism (Sw1 or S2) occurs, the following process is helpful: 1) Determine the substitution (methyl, 1º, 2º, or 3º) of the alkyl halide 2) Determine the strength of...
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary,...
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary, or tertiary, Label the nucleophile as strong or weak. Decide whether an S2 or an Sol reaction occurs. Alter, show the mechanism and product or products. Indicate stereochemistry where appropriate. a. Reaction of 1-bromopropane and sodium methoxide in methanol + Na CH₂ CH OH b. Reaction of 2-bromopropane in ethanol Br + CH.CH, OH - c. Reaction of (R) 3-chloro-3-methylheptane in acetic acid CH3...
5. REACTIONS (30PTS, 6PT EA): For the following reactions indicate what substituted alkyl halide sol are...
5. REACTIONS (30PTS, 6PT EA): For the following reactions indicate what substituted alkyl halide sol are provided and choose indicated reaction conditions, 2) then provide the major product or indicate dicate what substituted alkyl halide, solvent, and nucleopa cmajor product or indicate NO REACTION Closed Inuci NaOEt alkoi halide: 1.1.3 Salt Polar Proti Polar Agrote Noclegile strong wak Br EtOH Of Shade one — SI E2 S 2 EI Circle one cach alky balide 1º, 2º, 3º Solvent Polar Prote/Polar...
Please answer in detail 1. Classify the following cation, alkyl halide, and alcohol as either primary...
Please answer in detail
1. Classify the following cation, alkyl halide, and alcohol as either primary (1°), secondary (2º), tertiary (39) or но"
2. Classify the following alkyl halides as primary, secondary, or tertiary. Which one of these options...
2. Classify the following alkyl halides as primary, secondary, or tertiary. Which one of these options would be best suited for a unimolecular nucleophilic substitution reaction? مو لہ کی لہ لا 3. Describe the following reactions in written form, making sure to use the following terms where appropriate: nucleophile, lone pair, loss of leaving group, electron-deficient, and electrophile. . و ». . که ملیہ -- « -
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;
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary, or tertiary. Labe...
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary, or tertiary. Label the nucleophile as strong or weak. Decide whether an SN2 or an Sy1 reaction occurs. After, show the mechanism and product or products. Indicate stereochemistry where appropriate. a. Reaction of 1-bromopropane and sodium methoxide in methanol CH3 Na CH,Oн Br b. Reaction of 2-bromopropane in ethanol CH3CH2OH Br c. Reaction of (R) 3-chloro-3-methyl heptane in acetic acid Ci Cн CH,COOH но...
1. Which of the following structures is/are a secondary alkyl halide? (a) I and II (b)...
1. Which of the following structures is/are a secondary alkyl
halide? (a) I and II (b) II and V (c) I, II and V (d) IV only (e)
I, II and III 2. Which of the following is/are aprotic solvent(s)?
Choose all correct answers. (a) (b) (c) (d) (e) (f) 3. Which of the
following carbocations, if formed, is (are) likely to undergo
rearrangement through a hydride shift? (a) I (b) II (c) III (d) I
and II (e) II...
17. Which of the following statements is true? A. An Sw1 reaction always proceeds faster than...
17. Which of the following statements is true? A. An Sw1 reaction always proceeds faster than an S2 reaction. B. An Sw2 reaction is not stereospecific C. Good alkyl halide substrates for an E1 reaction are also good for an E2 reaction. D. Increasing the alkyl halide concentration enhances the reaction rate of an Sw1 reaction but not that of an E2 reaction. 18. For the following reaction, what happens to the reaction rate if the concentration of NaN, is...
2 Rob page 6 Part B: 3 1. Classify the following cation, alkyl halide, and alcohol...
2 Rob page 6 Part B: 3 1. Classify the following cation, alkyl halide, and alcohol as either primary (1"), secondary (2) or tertiary (3) HO 2. Write the major product(s) A, B and C for the following transformations: RUBH NaOH, HO2 С Br2 NaOH ( excess) B А
Please fill out the following table, indicating the category of reaction (Swi or Sm2) that will occur in each set of alkyl halides and nucleophiles. If no reaction occurs, write 'NR." Alkyl Halide Strong Nucleophile Weak Nucleophile SN2 SNZ SN2 SNI SNL SNU SNI SNI Methyl 10 2° 3° When determining which mechanism (Sw1 or S2) occurs, the following process is helpful: 1) Determine the substitution (methyl, 1º, 2º, or 3º) of the alkyl halide 2) Determine the strength of...
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary, or tertiary, Label the nucleophile as strong or weak. Decide whether an S2 or an Sol reaction occurs. Alter, show the mechanism and product or products. Indicate stereochemistry where appropriate. a. Reaction of 1-bromopropane and sodium methoxide in methanol + Na CH₂ CH OH b. Reaction of 2-bromopropane in ethanol Br + CH.CH, OH - c. Reaction of (R) 3-chloro-3-methylheptane in acetic acid CH3...
5. REACTIONS (30PTS, 6PT EA): For the following reactions indicate what substituted alkyl halide sol are provided and choose indicated reaction conditions, 2) then provide the major product or indicate dicate what substituted alkyl halide, solvent, and nucleopa cmajor product or indicate NO REACTION Closed Inuci NaOEt alkoi halide: 1.1.3 Salt Polar Proti Polar Agrote Noclegile strong wak Br EtOH Of Shade one — SI E2 S 2 EI Circle one cach alky balide 1º, 2º, 3º Solvent Polar Prote/Polar...
Please answer in detail
1. Classify the following cation, alkyl halide, and alcohol as either primary (1°), secondary (2º), tertiary (39) or но"
2. Classify the following alkyl halides as primary, secondary, or tertiary. Which one of these options would be best suited for a unimolecular nucleophilic substitution reaction? مو لہ کی لہ لا 3. Describe the following reactions in written form, making sure to use the following terms where appropriate: nucleophile, lone pair, loss of leaving group, electron-deficient, and electrophile. . و ». . که ملیہ -- « -
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;
Substitution Problems I. In each of the problems below, label the alkyl halide as primary, secondary, or tertiary. Label the nucleophile as strong or weak. Decide whether an SN2 or an Sy1 reaction occurs. After, show the mechanism and product or products. Indicate stereochemistry where appropriate. a. Reaction of 1-bromopropane and sodium methoxide in methanol CH3 Na CH,Oн Br b. Reaction of 2-bromopropane in ethanol CH3CH2OH Br c. Reaction of (R) 3-chloro-3-methyl heptane in acetic acid Ci Cн CH,COOH но...
1. Which of the following structures is/are a secondary alkyl
halide? (a) I and II (b) II and V (c) I, II and V (d) IV only (e)
I, II and III 2. Which of the following is/are aprotic solvent(s)?
Choose all correct answers. (a) (b) (c) (d) (e) (f) 3. Which of the
following carbocations, if formed, is (are) likely to undergo
rearrangement through a hydride shift? (a) I (b) II (c) III (d) I
and II (e) II...
17. Which of the following statements is true? A. An Sw1 reaction always proceeds faster than an S2 reaction. B. An Sw2 reaction is not stereospecific C. Good alkyl halide substrates for an E1 reaction are also good for an E2 reaction. D. Increasing the alkyl halide concentration enhances the reaction rate of an Sw1 reaction but not that of an E2 reaction. 18. For the following reaction, what happens to the reaction rate if the concentration of NaN, is...
2 Rob page 6 Part B: 3 1. Classify the following cation, alkyl halide, and alcohol as either primary (1"), secondary (2) or tertiary (3) HO 2. Write the major product(s) A, B and C for the following transformations: RUBH NaOH, HO2 С Br2 NaOH ( excess) B А
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