Ruby Allen
Organic Chemistry teacher | Experienced educator in USA
I specialize in Organic Chemistry, holding a degree from Tuskegee University. Passionate about illuminating the intricacies of this fascinating subject, I bring a wealth of knowledge and hands-on experience to answer your questions. As your guide through the world of organic compounds, I aim to simplify complex concepts and foster a deep understanding. Let's embark on this learning journey together, where no question is too challenging.
Questions
What are the advantages and disadvantages of mass spectroscopy?
What is a staggered conformer in a Newman projection?
What functional groups are found in proteins?
How many straight-chain isomers are there of hexene, #C_6H_12#?
How do you name halides?
What is the expected major product/products arising from the reaction of methylpropene with dilute potassium permanganate?
What does the prefix n- mean in orgo nomenclature?
Why are pi bonds more reactive?
Why is ethylene oxide dangerous?
How do you identify the compound with IR spectrum with a molecular formula #C_5H_8O#?
How do you write a net ionic equation for the reaction that occurs when aqueous solutions of sodium hydroxide and hydrofluoric acid are combined?
How do you classify alkanes, alkenes and alkynes?
How many single covalent bonds can carbon form?
Is it possible to draw Lewis dot diagrams for ionic compounds?
If the ring closure is an #S_N2# reaction then what should be the arrangement of the #-O-C-C-X# system?
How does NMR spectroscopy work?
What is an antimarkovnikov halogenation?
Why is benzene planar and cyclohexane nonplanar?
How do we name alkanes?
What is the Lewis Structure for iodoethane (#C_2H_5I#)?