· SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and

Page 1 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=1' data-page='1' class='cut-thumb lazyload' alt='Page 1: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/1.jpg' width='140' height='200' /> Page 2 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=2' data-page='2' class='cut-thumb lazyload' alt='Page 2: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/2.jpg' width='140' height='200' /> Page 3 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=3' data-page='3' class='cut-thumb lazyload' alt='Page 3: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/3.jpg' width='140' height='200' /> Page 4 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=4' data-page='4' class='cut-thumb lazyload' alt='Page 4: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/4.jpg' width='140' height='200' /> Page 5 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=5' data-page='5' class='cut-thumb lazyload' alt='Page 5: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/5.jpg' width='140' height='200' /> Page 6 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=6' data-page='6' class='cut-thumb lazyload' alt='Page 6: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/6.jpg' width='140' height='200' /> Page 7 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=7' data-page='7' class='cut-thumb lazyload' alt='Page 7: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/7.jpg' width='140' height='200' /> Page 8 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=8' data-page='8' class='cut-thumb lazyload' alt='Page 8: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/8.jpg' width='140' height='200' /> Page 9 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=9' data-page='9' class='cut-thumb lazyload' alt='Page 9: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/9.jpg' width='140' height='200' /> Page 10 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=10' data-page='10' class='cut-thumb lazyload' alt='Page 10: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/10.jpg' width='140' height='200' /> Page 11 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=11' data-page='11' class='cut-thumb lazyload' alt='Page 11: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/11.jpg' width='140' height='200' /> Page 12 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=12' data-page='12' class='cut-thumb lazyload' alt='Page 12: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/12.jpg' width='140' height='200' /> Page 13 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=13' data-page='13' class='cut-thumb lazyload' alt='Page 13: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/13.jpg' width='140' height='200' /> Page 14 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=14' data-page='14' class='cut-thumb lazyload' alt='Page 14: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/14.jpg' width='140' height='200' /> Page 15 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=15' data-page='15' class='cut-thumb lazyload' alt='Page 15: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/15.jpg' width='140' height='200' /> Page 16 <img data-url='document/-sn2-reactions-section-113-thus-the-leaving-group-x-in-the-alkylating-agent.html?page=16' data-page='16' class='cut-thumb lazyload' alt='Page 16: · SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and' loading='lazy' src='data:image/gif;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAYAAAAfFcSJAAAADUlEQVR42mNk+P+/HgAFhAJ/wlseKgAAAABJRU5ErkJggg==' data-src='https://reader043.cupdf.com/reader043/viewer/2022031006/5b896f367f8b9ae7298c6906/html5/thumbnails/16.jpg' width='140' height='200' />

· SN2 reactions (Section 11.3). Thus, the leaving group X in the alkylating agent can be chloride, bromide, iodide, or tosylate. Thc alkyl group R should be primary or methyl, and

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