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Michael J. S. Dewar

Michael J. S. Dewar 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 Michael J. S. Dewar rather than just read about it. In short: Michael James Steuart Dewar (24 September 1918 – 10 October 1997) was an American theoretical chemist. Education and early life Dewar was the son of Scottish parents, Annie Balfour (Keith) and Francis Dewar.

Michael J. S. Dewar — main illustration
Michael J. S. Dewar — illustration

Key takeaways

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

Reference excerpt

Michael James Steuart Dewar (24 September 1918 – 10 October 1997) was an American theoretical chemist.

Education and early life Dewar was the son of Scottish parents, Annie Balfour (Keith) and Francis Dewar. He received the degrees of Bachelor of Arts, Master of Arts, and DPhil from Balliol College, Oxford.

Career and research Dewar was appointed to the Chair in Chemistry at Queen Mary College of the University of London in 1951. He moved to the University of Chicago in 1959 and then to the first Robert A. Welch research chair at the University of Texas at Austin in 1963. After a long and productive period there, he moved to the University of Florida in 1989. He retired in 1994 as Professor Emeritus at the University of Florida. He died in 1997. Dewar's reputation for providing original solutions to vexing puzzles first developed when he was still a postdoctoral fellow at the University of Oxford. In 1945, he deduced the correct structure for stipitatic acid, a mould product whose structure had baffled the leading chemists of the day. It involved a new kind of aromatic structure with a seven-membered ring for which Dewar coined the term tropolone. The discovery of the tropolone structure launched the field of non-benzenoid aromaticity, which witnessed feverish activity for several decades and greatly expanded the chemists' understanding of cyclic π-electron systems. Also in 1945, Dewar devised the then novel notion of a π complex, which he proposed as an intermediate in the benzidine rearrangement. This offered the first correct rationalisation of the electronic structure of complexes of transition metals with alkenes, later known as the Dewar–Chatt–Duncanson model. In the early 1950s, Dewar wrote a famous series of six articles on a general Molecular orbital Theory of Organic Chemistry, which extended and generalised Erich Hückel's original quantum mechanical treatments by using perturbation theory and resonance theory, and which in many ways originated the modern era of theoretical and computational organic chemistry. Following Woodward and Hoffmann's suggestion of selection rules for pericyclic reactions, Dewar championed (concurrently with Howard Zimmerman) an alternative approach (which he erroneously felt had been pioneered by M. G. Evans) to understanding pericyclic reactivity based on aromatic and antiaromatic transition states. He did not however believe in the utility of Möbius aromaticity, introduced by Edgar Heilbronner in 1964, and now a flourishing area of chemistry. He is known most famously for the development in the 1970s and 1980s of the Semi-empirical quantum chemistry methods, MINDO, MNDO, AM1 and PM3 that are in the MOPAC computer program, and which for the first time enabled the quantitative study of the structure and mechanism of reaction (transition state) of many real (i.e. large) systems. This was illustrated in 1974 by computing (using the technique of energy minimisation) the structure of a molecule as large as LSD (with 49 atoms) at a quantum mechanical level (the calculation taking several days of the then state-of-the-art supercomputer time, a CDC 6600). It is worth noting that in 2006, the equivalent calculation takes less than 1 minute on a personal computer. In 2006, the same structure computation can now be completed using high-level ab initio or density functional procedures in less than two days, and semiempirical programs can be used to optimise the structures of molecules with perhaps 10,000 atoms. He was a member of the International Academy of Quantum Molecular Science.

Awards and honours His accolades include: Fellow of the American Academy of Arts and Sciences (1966); Member of the National Academy of Sciences (1983); Honorary Fellow, Balliol College, Oxford (1974); Tilden Medal of the Chemical Society (1954); Harrison Howe Award of the American Chemical Society (1961); Robert Robinson Medal, Chemical Society (1974); G.W. Wheland Medal of the University of Chicago (1976); Evans Award, The Ohio State University (1977); Southwest Regional Award of the American Chemical Society (1978); Davy Medal (1982); James Flack Norris Award of the American Chemical Society (1984); William H. Nichols Award of the American Chemical Society (1986); Auburn-G. M. Kosolapoff Award of the American Chemical Society (1988); Tetrahedron Prize for Creativity in Organic Chemistry (1989); WATOC Medal (World Association of Theoretical Organic Chemists Medal), (1990).

Personal life He is the father of Robert Dewar and C.E. Steuart Dewar.

References

Illustrations

Michael J. S. Dewar: Stipitatic acid
Stipitatic acid

Worked examples

Example 1 — a first encounter with Michael J. S. Dewar

Start with the simplest possible case. Write down what Michael J. S. Dewar 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 Michael J. S. Dewar 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 Michael J. S. Dewar 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 Michael J. S. Dewar

In research
Michael J. S. Dewar 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 Michael J. S. Dewar 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
Michael J. S. Dewar is common in secondary-school and first-year university syllabi. It links to neighbouring topics 1918 births, 1997 deaths, 20th-century American chemists, so understanding it makes those chapters shorter.
In everyday life
Look for Michael J. S. Dewar 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.
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How to study Michael J. S. Dewar in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Michael J. S. Dewar 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 Michael J. S. Dewar out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Michael J. S. Dewar in simple terms?

Michael James Steuart Dewar (24 September 1918 – 10 October 1997) was an American theoretical chemist. Education and early life Dewar was the son of Scottish parents, Annie Balfour (Keith) and Francis Dewar.

Why does Michael J. S. Dewar 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 Michael J. S. Dewar?

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 Michael J. S. Dewar.

Tags

  • 1918 births
  • 1997 deaths
  • 20th-century American chemists
  • Alumni of Balliol College, Oxford
  • American computational chemists
  • American fellows of the Royal Society
  • American theoretical chemists
  • British chemists
  • Chemists of Queen Mary University of London
  • Members of the International Academy of Quantum Molecular Science
  • University of Florida faculty

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