Regioselectivity - Study guides, Class notes & Summaries

CHEM 210 Reactions Test Questions and Answers All Correct Describe the mechanism for the electrophilic addition of a strong acid. - Answer-Step 1) An alkene grabs a hydrogen off of a strong acid, forming a carbocation intermediate. Step 2) The conjugate base of the acid (an anion now) bonds to the open shell carbocation What is the regioselectivity of electrophilic addition reactions? - Answer-Markovnikov What is Markovnikov regioselectivity? - Answer-States that the major product is d...

Organic Chemistry ACS Final Exam Study Guide Basicity rules - Answer--strong base: unstable/reactive (ED groups) -weak base: stable (EW groups/more EN/bigger) Chair conformation - Answer--more stable equitorial (slanted) -pointing up/pointing down=cis if both up -elimination: trans and diaxial Newman projection - Answer--gauche: substituent groups adjacent to eachother -grab middle and turn to put in plane Enantiomers - Answer--not superimposable mirror images -same besides stereochemi...

Organic chemistry notes on reaction of alkenes including hydrohalgenation, regioselectivity, hyperconjugation, carbocations, rearrangements, and more! Many practice problems and examples with detailed notes.

What is the degree of substitution? <<ANSWERS>>>The number of alkyl groups a specific carbon is bonded to (more alkyl groups means more stable) What reagents are required in a dissolving metal reduction? <<ANSWERS>>>Na or Li, ammonia (NH3) as solvent Provide a summary of dissolving metal reduction <<ANSWERS>>>2 hydrogens (one equivalent) are added to an alkyne to form the E alkene (anti addition) What is the stereochemistry of the dissolving ...

What is the degree of substitution? <<ANSWERS>>>The number of alkyl groups a specific carbon is bonded to (more alkyl groups means more stable) What reagents are required in a dissolving metal reduction? <<ANSWERS>>>Na or Li, ammonia (NH3) as solvent Provide a summary of dissolving metal reduction <<ANSWERS>>>2 hydrogens (one equivalent) are added to an alkyne to form the E alkene (anti addition) What is the stereochemistry of the dissolving ...

This study guide summarizes the key aspects of alkene addition reactions, including the reagents used, the regioselectivity (Markovnikov or anti-Markovnikov), and the products formed. The guide provides a concise summary of the reactions, with a focus on the functional groups added to the alkene and the stereochemistry of the addition. The reactions covered include hydrohalogenation, acid-catalyzed hydration, oxymercuration-reduction, hydroboration-oxidation, hydrohalogenation by free radicals, ...

Part 2 of Chapter 7 of Organic Chemistry 1 at App State (CHE2201) taught by Dr. Moeller. This chapter is very long so it is split into two parts. The second part of this chapter covers elimination, Zaitsev's rule, hyperconjugation, regioselectivity, cis & trans alkenes, Newman projections, and rearrangements. Some images/definitions are not entirely my own; credit for any work that is not mine goes to its rightful owners.

Chem 210 Exam II Questions and Correct Answers, Complete Solution 2024. electrophiles electron seeking reagents that have room to accept a electron pair nucleophiles reagents seeking a nucleus to which to donate a pair of electrons proton transfer or protonation reaction the transfer of a proton from one base to another transition state lying between the products and reactants free energy of activation (delta G double dagger) the height of the barrier, the energy that the reactants a...

Chapters 12 and 13 wrap up the Organic Chemistry 1 class. We begin Chapter 12 to learn about alcohols and phenols. Students should already have extensive knowledge about alkanes, alkenes and alkynes. They will then learn how the IUPAC name for alcohols differs slightly. They will also learn about oxidation and reduction reactions and how to recognize one. Additionally, students will learn about Grignard reagents and how they contribute to oxidation and reduction reactions. It is also important f...

Organic Chemistry 1 covers Lewis structures, types of bonding, VSEPR Theory, molecular polarity, dipoles and electronegativity, intermolecular forces, solubility, condensed and bond-line structures and various molecular groups (i.e. arene, ketone), resonance forms, acid and base chemistry, chirality and chiral centers, enantiomers, constitutional isomers, stereospecific compounds, substitution and elimination reactions, leaving groups, nucleophilic compounds, halide classification, reaction rate...