Paisley Boney
Organic Chemistry teacher | Verified Expert
I hold a graduate degree in Organic Chemistry from Davenport University. With a profound understanding of chemical structures and reactions, I excel in simplifying complex concepts for my students. My passion lies in fostering a deep appreciation for the intricacies of organic chemistry, guiding learners to grasp fundamental principles with clarity and confidence. Whether unraveling the mysteries of functional groups or elucidating reaction mechanisms, I am dedicated to empowering students to succeed in their academic endeavors. Join me on a journey of discovery and mastery in the fascinating realm of organic chemistry.
Questions
What is the Dirac vector model in NMR?
Why are cycloalkanes useful?
How do carbocations form?
Why do primary alkyl halides typically undergo SN2 substitution reactions more rapidly?
What are the possible resonance structures of #CH_3-CH=CH-CH=O# and #CH_3-COO^-#? What is the order of stability of the contributing resonance structures?
What factors affect coupling constants?
Why don't bromide ions react with methoxide ions?
Why is isopropyl alcohol soluble in water?
Why do London forces occur?
Why is halogenation of an alkane a substitution reaction?
How can I draw the more stable chair conformer of cis -1-ethyl-2-methylcyclohexane?
Can diastereomers be separated?
What does infrared spectroscopy tell you?
How can you isolate optical isomers?
How is IR spectroscopy read?
How do you write anhydride formulas?
Why is cis–trans isomerism common in alkenes?
Can some one help me with this question ??
Why are magnets dipoles?
What are the major products for reaction with cis-1-chloro-3-methylcyclopentane and trans-1-chloro-3-methylcyclopentane with #"OH"^(-)# in water at high temperature?