Santiago Alfonso
Organic Chemistry teacher | Verified Expert
With a passion for Organic Chemistry ignited during my studies at Western University of Health Sciences, I bring a depth of knowledge and enthusiasm to each tutoring session. My goal is to make complex concepts digestible and enjoyable, fostering a deeper understanding of the subject. From reaction mechanisms to synthesis strategies, I'm here to guide students through every step of their learning journey. Let's unravel the mysteries of Organic Chemistry together and pave the way for academic success.
Questions
What is the Bronsted-Lowry acid and base versus Lewis?
What is an acid-base reaction?
Which of the following compounds is most reactive to an aqueous solution of sodium carbonate ?
If D- and L- glucose are enantiomers, are D- and L-fructose not enantiomers?
How do you do addition reactions of alkenes?
What are the chiral centers in ephedrine?
Is an ether a #"Lewis base"#?
What is electrophilic aromatic substitution?
How do you know which mixture of products are favoured when phenol is brominated?
What can I do to prepare for organic chemistry lab?
What are the cis and trans isomers for cyclohexane?
Are D-fructose and L-fructose anomers, epimers, diastereomers, enantiomers, or not stereoisomers?
Is phenol more acidic than menthol?
Why is osmium tetroxide used in organic chemistry?
Why is sulfide a better nucleophile than the structurally equivalent alkoxide?
What is alkyl chloride?
What does the oxidation of a primary alcohol produce?
What is a methyl ketone?
What is the chemical equation for the decarboxylation of butyric acid with soda lime?
Why is the #pi# bond between the two central carbon atoms destroyed halfway through the rotation from cis- to trans-2-butene?