{"title":"初始化","authors":"","doi":"10.1163/9789004488380_004","DOIUrl":null,"url":null,"abstract":"1. explain why the radical halogenation of alkanes is not usually a particularly good method of preparing pure samples of alkyl halides. 2. use \\(\\ce{\\sf{C–H}}\\) bond energies to account for the fact that in radical chlorinations, the reactivity of hydrogen atoms decreases in the order \\[\\text{tertiary} > \\text{secondary} > \\text{primary}.\\] 3. predict the approximate ratio of the expected products from the monochlorination of a given alkane.","PeriodicalId":129263,"journal":{"name":"Out of the Cradle Endlessly Rocking","volume":"12 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2005-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Initiation\",\"authors\":\"\",\"doi\":\"10.1163/9789004488380_004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"1. explain why the radical halogenation of alkanes is not usually a particularly good method of preparing pure samples of alkyl halides. 2. use \\\\(\\\\ce{\\\\sf{C–H}}\\\\) bond energies to account for the fact that in radical chlorinations, the reactivity of hydrogen atoms decreases in the order \\\\[\\\\text{tertiary} > \\\\text{secondary} > \\\\text{primary}.\\\\] 3. predict the approximate ratio of the expected products from the monochlorination of a given alkane.\",\"PeriodicalId\":129263,\"journal\":{\"name\":\"Out of the Cradle Endlessly Rocking\",\"volume\":\"12 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Out of the Cradle Endlessly Rocking\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1163/9789004488380_004\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Out of the Cradle Endlessly Rocking","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1163/9789004488380_004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
1. explain why the radical halogenation of alkanes is not usually a particularly good method of preparing pure samples of alkyl halides. 2. use \(\ce{\sf{C–H}}\) bond energies to account for the fact that in radical chlorinations, the reactivity of hydrogen atoms decreases in the order \[\text{tertiary} > \text{secondary} > \text{primary}.\] 3. predict the approximate ratio of the expected products from the monochlorination of a given alkane.