ArticleslgStudy

chemistry

James M. Bobbitt

James M. Bobbitt is a chemistry topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand James M. Bobbitt rather than just read about it. In short: James McCue Bobbitt (January 18, 1930 – November 22, 2021) was an American chemist and academic who taught chemistry at the University of Connecticut from 1956 to 1991 and developed the Bobbitt reaction. Early life and education Bobbitt was born on January 18, 1930, in Charleston, West Virginia, to parents James Sterling Bobbitt and Grace McCue Bobbitt.

James M. Bobbitt — main illustration
James M. Bobbitt — illustration

Key takeaways

  • James M. Bobbitt belongs to chemistry; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect James M. Bobbitt to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of James M. Bobbitt from memory before moving on to harder problems.

Reference excerpt

James McCue Bobbitt (January 18, 1930 – November 22, 2021) was an American chemist and academic who taught chemistry at the University of Connecticut from 1956 to 1991 and developed the Bobbitt reaction.

Early life and education Bobbitt was born on January 18, 1930, in Charleston, West Virginia, to parents James Sterling Bobbitt and Grace McCue Bobbitt. He earned a Bachelor of Science degree in chemistry from West Virginia University in 1951 and a PhD from Ohio State University in 1955, working with Melville L. Wolfrom on periodate oxidations.

Research and career Bobbitt worked from 1952 to 1955 as a teaching assistant at Ohio State. He then moved to Wayne State University, as a postdoctoral fellow in the research group of Carl Djerassi, working on isoquinoline alkaloids. In 1956, he was hired as a lecturer at the University of Connecticut where he became professor of chemistry from 1969 to 1991. He served as Department Head of Chemistry from 1956 to 1972. In 1992 he became professor emeritus but continued to work in the laboratory, with a focus on oxidation chemistry. In 1959, he received a National Science Foundation fellowship to work with Hans Schmid at the University of Zürich in Switzerland on iridoid glycosides. Bobbitt also worked as a visiting lecturer; from 1964 to 1965 at the University of East Anglia under the direction of Alan R. Katritzky; in June 1968 with a short DAAD grant at the University of Kiel with Burchard Franck; from 1971 to 1990 in a collaboration with Tohoku University in Sendai, Japan with Tetsuji Kametani and Tetsuo Osa on catalytic oxidations; and at La Trobe University in Australia from 1980 to 1981 and at the University of Adelaide in 1985. His research focused on alkaloids, preparative electrochemistry, and oxidation chemistry. Additional research interests included the synthesis of nitrogen heterocycles, thin-layer chromatography, electrolytic oxidation and oxoammonium salt oxidation of alcohols with stoichiometric amounts of Bobbitt's salt. He developed what became known as the Bobbitt reaction for the synthesis of tetrahydroisoquinoline and its derivatives in 1965. In 1968, Bobbitt became lead instructor for an American Chemical Society course on thin-layer chromatography and taught seminars across the US on that subject. In 1970, he became president of the UConn Sigma Xi chapter, and in 1975, the president of the UConn Phi Beta Kappa chapter.

Personal life Bobbitt met his wife, Jane Ann Hickman, while they were both students at West Virginia University. They had three children: John, Annie, and Laura. In retirement, Bobbitt made wine, raised bees, and gardened, but he remained active in the laboratory and writing papers well into his 80s. Bobbitt was critically injured in a car crash on November 22, 2021, in Windham, Connecticut. He died hours later at Hartford Hospital.

Books and selected papers Bobbitt was the author of two books on chromatography and some 120 research articles.

Books James M. Bobbitt: Thin-layer Chromatography. Reinhold Publishing Co., New York 1963. J. M. Bobbitt, A. E Schwarting, and R. J. Gritter, Introduction to Chromatography. Reinhold Publishing, Co. New York (1968), Second Edition, R. J. Gritter, J. M. Bobbitt and A. E. Schwarting, Holden-Day, Inc., Oakland California.

Reviews J. M. Bobbitt: Periodate Oxidations of Carbohydrates, Advances in Carbohydrate Chemistry, Vol. 11, 1956, 1-42. J. M. Bobbitt: The Chemistry of 4-Oxy- and 4-keto-1,2,3,4-tetrahyhdroisoquinolines, Advances in Heterocyclic Chemistry, Vol. 15, 1973, 99-128. (The Bobbitt Reaction). J. M. Bobbitt, A. J. Bourque: Syntheses of heterocycles using aminoacetals, Heterocycles. Vol. 25, 1987, pp. 601–616. J. M. Bobbitt and K.-P. Segebarth: The Iridoid Glycosides and Similar Substances, in Cyxlopentanoterpine Derivatives, W. I. Taylor and A. R. Battersby, Eds. Marcel Dekker, 1969, 1-139. T. Osa, Y. Kashiwagi, J. M. Bobbitt, and Z. Ma: Electroorganic Synthesis on Catalyst Coated Electrodes. In Electronic Synthesis, R. D. Little and N. L. Weinberf, Eds., Marcel Dekker, Inc. New York, 343-354.1991. J. M. Bobbitt, C. Brückner and N. Merbouh: Oxoammonium Salt and Nitroxide Catalyzed Oxidations of Alcohols. Organic Reactions, Vol. 74, 2009 103-424.

Selected papers M. L Wolfrom, J. M. Bobbitt: Periodate oxidation of cyclic 1,3, -diketones. Journal of the American Chemical Society Vol. 78, 1956, 2489. C. Djerassi, S. K. Figdor, J. M. Bobbitt, F. I. Markley: Alkaloid studies. XIV. The structure of the cactus alkaloid piloceriene. Journal of the American Chemical Society. Volume 78, 1956, 3861. J. M. Bobbitt, H. Schmid, T. B. Africa. Catalpa glycosides. 1. The chararctization of catalposide. Journal of Organic Chemistry Vol. 26, 1961, 2230. J. M. Bobbitt, J. C. Sih: Synthesis of isoquinolines. VII. 4-hydroxy-1,2,3,4-tetrahydroisoquinolines. Journal of Organic Chemistry. Vol. 33, 1968, 856-859. J. M. Bobbitt, A. R. Katritzky, R. D. Kennewell, M. Snarey: Steric requirements of sp2-Hybridized lone electron pairs. Part 1. The conformation of –(pyridylmethylene-onesnes. J. Chem. Soc (B) 1968, 550-553. J. M. Bobbitt, A. S. Steinfeld, K. H. Weisgraber, S. Dutta: Synthesis of isoquinolines. X. 1-alkyl-1,2,3,4-tetrahydroisoquinoilines. in:Journal of Organic Chemistry. Vol. 34, 1969, 2487. J. M. Bobbitt, I. Noguchi, H. Yagi, K. H. Weisgraber: Electrochemistry of natural Products. III. A stereoselective, stereospecific phenol coupling reaction. In: Journal of the American Chemical Society 1971, 93, 551. J. M. Bobbitt, S. J. Huang: A simulated research project in synthetic organic chemistry. An undergraduate laboratory. In: J. Chem. Educ. Volume 51, 1974, 58. J. M. Bobbitt, I. G. C. Coutts, M. R. Hamblin, E.J. Tinley: The enzymatic oxidation of phenolic tetrahydroisoquinoline-1-carboxylic acids. In: Journal of the Chemical Society, Perkin Transactions 1, 1979, pp 2744–2749.

References

External links Media related to James M. Bobbitt at Wikimedia Commons

Illustrations

James M. Bobbitt illustration

Worked examples

Example 1 — a first encounter with James M. Bobbitt

Start with the simplest possible case. Write down what James M. Bobbitt claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In chemistry, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to James M. Bobbitt before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about James M. Bobbitt ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of James M. Bobbitt

In research
James M. Bobbitt appears in chemistry research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses James M. Bobbitt in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
James M. Bobbitt is common in secondary-school and first-year university syllabi. It links to neighbouring topics 1930 births, 2021 deaths, 20th-century American chemists, so understanding it makes those chapters shorter.
In everyday life
Look for James M. Bobbitt outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
Ask Teacher Smith questions about this articleOpens your AI tutor with a question about “James M. Bobbitt” →

Affiliate

Preply — study more efficiently by working with a personal tutor. 50% off.

How to study James M. Bobbitt in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what James M. Bobbitt means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain James M. Bobbitt out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is James M. Bobbitt in simple terms?

James McCue Bobbitt (January 18, 1930 – November 22, 2021) was an American chemist and academic who taught chemistry at the University of Connecticut from 1956 to 1991 and developed the Bobbitt reaction. Early life and education Bobbitt was born on January 18, 1930, in Charleston, West Virginia, to…

Why does James M. Bobbitt matter?

Because it connects several chemistry ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study James M. Bobbitt?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on James M. Bobbitt.

Tags

  • 1930 births
  • 2021 deaths
  • 20th-century American chemists
  • 20th-century American educators
  • American organic chemists
  • Chemists from West Virginia
  • Ohio State University College of Arts and Sciences alumni
  • Road incident deaths in Connecticut
  • Scientists from Charleston, West Virginia
  • University of Connecticut faculty
  • West Virginia University alumni

Keep exploring