


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 information do we get from analyzing 2D NMR spectra?
What is an alkoxy group?
How can I compare the staggered conformer and eclipsed conformers for (ethane) #H_3C- CH_3# in Newman projections?
Which of the following mechanisms feature carbocation intermediates: SN1 only, SN2 only, E1 only, E2 only or both SN1 and E1?
What is the difference between an identical and a structural isomer?
What are primary alcohols oxidized to form?
How many chiral centres are in the penicillin molecule?
What happens when alkenes are oxidized?
How can I convert the bond line view of L-idose to a Fischer projection?
How can I draw possible structures for an ester that has a molecular ion with an m/z value of 74?
Why is aldehyde a reducing agent?
What is a functional group in organic chemistry?
Draw the Lewis structure for the molecule #CH_2CHCH_3#. How many sigma and pi bonds does it contain?
How many structural isomers can be drawn for the formula #C_3H_8#?
How many single bonds are in a propane molecule?
What are some common mistakes students make with skeletal structures in organic chemistry?
What carbocation is most stable?
Why is phenoxide ion a stronger acid than alkoxide ion?
What are #S_N1, S_N2, E1 and E2# reactions? How to identify which reaction is occurring in any given reaction.
How many geometric isomers are there for the following compound? #[Mn(CO)_2Cl_2Br_2]^+#?