Sn1 Study guides, Class notes & Summaries

Which reagent is not an oxidizing agent? a. NaOCl b. KMnO4 c. K2Cr2O7 d. CrO3 e. H2O - H2O Which statement is false about preparing alkyl halide from alcohol with hydrogen halide? a. it is an SN1 reaction b. tertiary alcohols react faster than secondary alcohols c. the intermediate is a carbocation d. alkyl halide is soluble in conc. HCl e. in the reaction, the slowest step is the formation of a carbocation - alkyl halide is soluble in conc. HCl 2‐Chloro‐2‐methylpentane was tr...

Reagent = Nucleophile Only - ANSWER1° = Sn2 2° = Sn2 3° = Sn1 + E1 (polar medium necessary) Reagent = Strong Nucleophile & Strong Base - ANSWER1° = Sn2 2° = E2 3° = E2 Reagent = Weak Nucleophile and Weak Base - ANSWER1°/2° = No Reaction 3°/resonance stabilized carbocation = Sn1 + E1 (polar medium necessry Reagent = Base Only - ANSWER1° = E2 or Sn2 (if unhindered and no beta-hydrogen with unhindered base) 2° = E2 3° = E2 Examples of Only Nucleophiles - ANSWERCl⁻, ...

CHEM 334 Final Exam Questions and Answers, Latest Updated 2024/2025 | 100% Correct Answers. Write accurate structures for the following: CHEM 334 Final Exam Questions and Answers, Latest Updated 2024/2025 | 100% Correct Answers 8/6/22, 10:11 PM Final Exam 2/4 a) the conjugate base of 1-propyne b) a compound of formula C3H4O with ONLY sp2 carbons c) a good 3-dimensional structure for NH2OH (including lone pairs) d) a Newman diagram of anti 1-propanol e) a bicycloheptane of formula C7H12...

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SN1 Reaction - ANSWER- Unimolecular nucleophilic substitution - 2 steps - Starting with enantiomerically pure product tends to result in some degree of racemization - Retention AND inversion at stereocenter (R and S) - 1 nucleophile is replaced by another nucleophile - Carbocation INTERMEDIATE forms - Rate is dependent only on substrate concentration 1. LG leaves, forming a carbocation 2. Nucleophile attacks the carbocation, forming the product SN2 Reaction - ANSWER- Bimolecular nuc...

Orgo Synthesis Questions & Answers A+ Review Alcohol Synthesis from Methyl - ANS-NaOH (SB) --> Sn2 Substitution of OH and LG Alcohol Synthesis from 1*C - ANS-NaOH (SB) --> Sn2 Substitution of OH and LG Alcohol Synthesis from 2*C - ANS-Na(OAc) + NaOH --> SnAc Substitution of OH and LG Alcohol Synthesis from 3*C - ANS-H20 (WB) --> Sn1 Substitution of OH and LG (C+ Rearrangement) Alcohol Elimination (Dehydration) from Methyl - ANS-No reaction Alcohol Elimination (Dehydration)...

CHEM 334 Final Exam Questions and Answers, Latest Updated 2024/2025 | 100% Correct Answers. Write complete names for each of the following, including stereochemistry if it is specifically shown. a) b) c) d) e) 2. (15 points) Write accurate structures for the following: CHEM 334 Final Exam Questions and Answers, Latest Updated 2024/2025 | 100% Correct Answers 8/6/22, 10:11 PM Final Exam 2/4 a) the conjugate base of 1-propyne b) a compound of formula C3H4O with ONLY sp2 carbons c) a...

Reagent = Nucleophile Only - ANSWER1° = Sn2 2° = Sn2 3° = Sn1 + E1 (polar medium necessary) Reagent = Strong Nucleophile & Strong Base - ANSWER1° = Sn2 2° = E2 3° = E2 Reagent = Weak Nucleophile and Weak Base - ANSWER1°/2° = No Reaction 3°/resonance stabilized carbocation = Sn1 + E1 (polar medium necessry Reagent = Base Only - ANSWER1° = E2 or Sn2 (if unhindered and no beta-hydrogen with unhindered base) 2° = E2 3° = E2 Examples of Only Nucleophiles - ANSWERCl⁻, ...

Is SN2 concerted or stepwise correct answer: Concerted Is SN1 concerted or stepwise correct answer: Stepwise When is there a change in configuration in an SN2 correct answer: When alpha position is a chiral center What type of substrate reacts most quickly for SN2 correct answer: Primary What type of substrate reacts most quickly for SN1 correct answer: Tertiary (bc more stable carbocation) What type of nucleophiles favor SN2 correct answer: Strong List 9 strong nucleophi...

UMICH CHEM 210 - Exam #3 - Reaction Mechanisms 100% Correct SN1 Reaction - ANSWER- Unimolecular nucleophilic substitution - 2 steps - Starting with enantiomerically pure product tends to result in some degree of racemization - Retention AND inversion at stereocenter (R and S) - 1 nucleophile is replaced by another nucleophile - Carbocation INTERMEDIATE forms - Rate is dependent only on substrate concentration 1. LG leaves, forming a carbocation 2. Nucleophile attacks the carbocati...