Sn2 reaction - Study guides, Class notes & Summaries

Chapter 3 -- Alkenes and Alkynes MULTIPLE CHOICE 1. Which of the following dienes can be classified as conjugated? A) CH3CH=C=CH2 B) CH3CH=CHCH=CH2 C) CH2=CHCH2CH=CH2 D) CH3CH=CHCH2CH2CH=CH2 E) CH2=C=CH2 ANS: B TOP: Alkenes and Alkynes: Nomenclature and Structure 2. Which of the following molecular formulas could not represent an alkene? A) C5H10 B) C7H14 C) C10H20 D) C27H56 E) C31H62 ANS: D TOP: Alkenes and Alkynes: Nomenclature and Structure 3. What...

what factors explain the outcomes of reactions? - hybridization, delocalization, eN, atom density what is a leaving group? - - group of atom(s) that can be stable on its own - eN atoms that are good LG also make strong acids what is the α carbon? - C directly attached to leaving group what are β Cs? β Hs? - βC: C(s) attached to α carbon βH: H(s) attached to βC what is a LB? is it a nucleophile or electrophile? - lewis base, nucleophile what is nucleophilic ...

Objective: To examine the use of a phase transfer catalyst to effect an SN2 reaction in dichloromethane solution. The reaction will be conducted without extraction for product isolation. List the procedural steps, from start to finish, that are required to convert 2-naphthol and allyl bromide into allyl 2-naphthyl ether. - The reaction is performed on a small scale by mixing the alcohol, the haloalkane, and the phase transfer catalyst in a conical vial. Sodium hydoxide (base) is added to ini...

Chem 210 Exam 3 Questions and Correct Answers, With Complete Solution. what face of the pi bond can EAR occur from? either face how many products do EARs on an alkene form? 4 stereoisomeric products Brainpower Read More in a substitution rxn, what does H-O act as? nucleophile and replaces LG in an elimination rxn, what does H-O acts as? base and abstracts BH atom what is a requirement for elimination rxns? beta hydrogen what is a requirement for substitution rxns? leaving group ...

AAMC FL 1 Exam Questions and Answers 2024 If Reaction 2 (Figure 4) is repeated with HCl and the compound shown below, which of the following compounds is NOT a direct product (without rearrangement)? -Answer-Compound A requires a hydride shift to form- therefore not a direct product. NOT an SN2 reaction because of tertiary alcohol- it is SN1 What is the energy of the photons emitted by the LED at a frequency of 610 THz? (Note: h = 6.6 × 10-34 J·s) -Answer-The photon energy is the energy...

In the chromatography of the reaction mixture, water absorbed on cellulose functioned as the stationary phase. What was the principal factor determining the migration of individual components in the sample? A.Hydrogen bonding B.Solute concentration C.Stationary phase concentration D.Thickness of paper The correct answer is A. This is an Organic Chemistry question that falls under the content category "Separation and purification methods." The answer to this question is A because the ...

Chem 210 Exam 3 Questions and Correct Answers, With Complete Solution. what face of the pi bond can EAR occur from? either face how many products do EARs on an alkene form? 4 stereoisomeric products Brainpower Read More in a substitution rxn, what does H-O act as? nucleophile and replaces LG in an elimination rxn, what does H-O acts as? base and abstracts BH atom what is a requirement for elimination rxns? beta hydrogen what is a requirement for substitution rxns? leaving group ...

Organic Chemistry Lab I (CHEM 237) Experiment 10: Phase Transfer Catalysis 100% Correct List the procedural steps, from start to finish, that are required to convert 2-naphthol and allyl bromide into allyl 2-naphthyl ether. The reaction is performed on a small scale by mixing the alcohol, the haloalkane, and the phase transfer catalyst in a conical vial. Sodium hydoxide (base) is added to initiate the reaction. The reaction flask is covered and stirred to conduct reaction to prevent evaporation...

regioisomers - Answer structural isomers formed in some reaction, same formula but different connectivities nucleophile - Answer e- sources drawn to positive centers, more negative [bases are all nucleophiles] in SN2, nucleophile attacks C sp3 only if C is having e- pulled away from it (partial positive charge) electrophile - Answer C sp3 with leaving group leaving group (LG) - Answer atoms/groups that pull away e-s good leaving groups: halogens and A+ bimolecular nucleophilic...

In the chromatography of the reaction mixture, water absorbed on cellulose functioned as the stationary phase. What was the principal factor determining the migration of individual components in the sample? A) Hydrogen bonding B) Solute concentration C) Stationary phase concentration D) Thickness of paper A) Hydrogen bonding The answer to this question is A because the relative amount of hydrogen bonding to the stationary phase will determine the relative rate of migration of the vario...