4.1.1 Basic concepts of organic chemistry
(f) the different types of covalent bond fission:
(i) homolytic fission (in terms of each bonding atom receiving one electron from the bonded pair, forming two radicals)
(ii) heterolytic fission (in terms of one bonding atom receiving both electrons from the bonded pair)
(g) the term radical (a species with an unpaired electron) and use of ‘dots’ to represent species that are radicals in mechanisms Radical mechanisms will be represented by a sequence of equations. Dots, •, are required in all instances where there is a single unpaired electron (e.g. Cl• and CH3•). Dots are not required for species that are diradicals (e.g. O). (h) a ‘curly arrow’ described as the movement of an electron pair, showing either heterolytic fission or formation of a covalent bond ‘Half curly arrows’ are not required, see 4.1.2 f. HSW1,8 Use of the ‘curly arrow’ model to demonstrate electron flow in organic reactions. (i) reaction mechanisms, using diagrams, to show clearly the movement of an electron pair with ‘curly arrows’ and relevant dipoles. Any relevant dipoles should be included. Curly arrows should start from a bond, a lone pair of electrons or a negative charge. HSW1,2,8 Use of reaction mechanisms to explain organic reactions.