000			02096nam a22002657a 4500
003			OSt
005			20250224113648.0
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020			_a9781839167430
040			_aNISER LIBRARY _beng _cNISER LIBRARY
082	0	4	_a547 _bZIP-R
100	1		_aZipse, Hendrik
245	1	0	_aReactivity and mechanism in organic chemistry
250			_a2nd edition.
260			_aLondon, UK : _bRoyal Society of Chemistry, _c2023.
300			_aviii, 195 pages : _billustrations (some color) ; _c24 cm
500			_aPreviously published by Shaker Verlag, 2019.
504			_aIncludes bibliographical references and index.
520			_aCompletely revised and updated, this 2nd Edition of Reactivity and Mechanism in Organic Chemistry is an ideal introduction to the quantitative description of organic reactivity for students in undergraduate and masters chemistry programmes. The book proceeds logically from qualitative molecular orbital theory as a tool for the description of bonding phenomena to combining this with thermochemical data to rationalise concepts such as molecular strain and hyperconjugation. Next, transition state theory, for examining organic reactivity phenomena, is introduced and its relation to energy surfaces and simple rate equations is discussed. On this basis more specific reactivity concepts commonly used in organic chemistry are explored such as the Bell–Evans–Polanyi principle, Marcus theory, HSAB principle, Hammett correlations, the Mayr–Patz equation, and FMO theory. How these reactivity models are applied is demonstrated for pericyclic reactions and selected rearrangement reactions involving transient intermediates such as radicals, diradicals, or carbocations, and for reactions involving classical electrophile/nucleophile combinations.
650		0	_aChemistry, Organic.
650		0	_aChemical reactions.
650		0	_aChemical processes.
856			_3Reviews _uhttps://www.goodreads.com/book/show/75665127-reactivity-and-mechanism-in-organic-chemistry?ref=nav_sb_ss_1_13#CommunityReviews
942			_2udc _cBK
999			_c35750 _d35750