Synthesis of Ethano Strapped TBs

Synthesis of Ethano Strapped TBs Chapter 3 Synthesis of Ethano Strapped TBs. 3.2  Experimental Section 3.2.1  General procedure for the synthesis of ethano-strapped Trà ¶gers base. The methano-strapped TrÓ §gers base (4.24 mmol) and 1,2-dibromoethane (1.60 g, 8.48 mmol, 2.0 eq.) were dissolved in N,N-dimethylformamide (5 mL) and lithium carbonate (1.41 g, 19.08 mmol, 4.5 eq.) was added to the mixture which was stirred and heated at 110  °C for 3 days.   The mixture was cooled and suspended in ethyl acetate (100 mL) and then washed with water (2 25 mL), dried over anhydrous magnesium sulfate, filtered and evaporated to dryness.   The crude material was chromatographed (silica gel) to afford the desired ethano-strapped Trà ¶gers base products. 3.3.5  2,8-Dimethoxy-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X(MHK 02-60)ACT checked NMR Starting with 2,8-dimethoxy TrÓ §gers base X (1.20 g, 4.24 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane:ethyl acetate 4:1) to afford X (659 mg, 53%) as an off-white solid.   m.p. 185-187  °C (lit.ref 186-189  °C)1.   1H NMR (400 MHz, CDCl3), ÃŽ ´ 3.55-3.61 (4H, m, CH2-CH2), 3.68 (6H, s, OCH3), 4.37 (2H, d, J = 17.2 Hz, CH2), 4.55 (2H, d, J = 17.2 Hz, CH2), 6.43 (2H, d, J = 2.8 Hz, ArH), 6.62 (2H, dd, J = 2.8, 8.6 Hz, ArH), 7.07 (2H, d, J = 8.6 Hz, ArH).   The data are in agreement with those reported in the literature.1 3.3.4  2,8-Dibromo-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X(MHK 01-120)ACT checked NMR Starting with 2,8-dibromo TrÓ §gers base X (1.65 g, 4.24 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane) to afford X (750 mg, 45%) as an off-white solid.   m.p. 220  °C.   1H NMR (400 MHz, CDCl3) ÃŽ ´ 3.47-3.59 (4H, m, CH2-CH2), 4.35 (2H, d, J = 17.4 Hz, CH2), 4.53 (2H, d, J = 17.4 Hz, CH2), 6.96 (2H, d, J = 8.4 Hz, ArH), 7.04 (2H, d, J = 2.1 Hz, ArH), 7.17 (2H, dd, J = 2.1, 8.4 Hz, ArH).   The data are in agreement with those reported in the literature.2 3.3.2  6H,12H-5,11-Ethanodibenzo[b,f][1,5]diazocine X(MHK 01-116)ACT checked NMR Starting with unsubstituted methano-strapped TrÓ §gers base X (942 mg, 4.24 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane: ethyl acetate 4:1) to afford X (505 mg, 51%) as an off-white solid.   m.p. 169-171  °C (lit.3 174  °C).   1H NMR (400 MHz, CDCl3) ÃŽ ´ 3.53-3.68 (4H, m, CH2-CH2), 4.46 (2H, d, J = 17.2 Hz, CH2), 4.61 (2H, d, J = 17.2 Hz, CH2), 6.89-6.96 (4H, m, ArH), 7.03-7.08 (2H, m, ArH), 7.09-13 (2H, m, ArH).   The data are in agreement with those reported in the literature.3 5.3.20Di-tert-butyl-3,9-dicarbamate-2,8-dimethyl-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X (MHK-06-108)   Sample has a lot of ethyl acetate in it re-run both 1H and 13C NMR Starting with bis(3,9-tert-butyl-dicarbamate-2,8-dimethyl TrÓ §gers base X (5.00 g, 10.42 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane:ethyl acetate 1:1) to afford X (2.67 g, 52% with 7% methano strapped as a impurity) as a pale brown solid.   m.p. X-Y  °C.   1H NMR (400 MHz, CDCl3) ÃŽ ´ 1.49 (18H, s, Boc CH3), 2.03 (6H, s, CH3), 3.50-3.60 (4H, m, CH2-CH2), 4.40 (2H, d, J = 17.1 Hz, CH2), 4.48 (2H, d, J = 17.1 Hz, CH2), 6.08 (2H, s, ArH), 6.67 (2H, s, ArH), 7.56 (2H, br s, NH).   13C NMR (100 MHz, CDCl3) ÃŽ ´ 17.1, 28.3, 54.9, 58.5, 80.2, 120.3, 128.4, 130.3, 132.0, 134.9, 148.8, 152.9 ppm.   FTIR 1049 (m), 1182 (s), 1230 (m), 1709 (s, C=O), 2900 (m), 2972 (m), 3295(bs), cm-1.   Anal. Calcd for C28H38N4O4:   C 67.99; H 7.74; N 11.33.   Found C XX; H XX; N XX %. 3.3.38H,16H-7,15-Ethanodinaphtho[2,1-b][2,1-f][1,5]diazocine X(MHK 03-72)ACT checked NMR contains an impurity ethano strap region should be symmetric Re-run both 1H and 13C NMR grow crystals! Starting with naphthalene TrÓ §gers base X (500 mg, 1.55 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane) to afford X (113 mg, 22%) as an off-white solid.   m.p. 224-227  °C.   1H NMR (400 MHz, CDCl3) ÃŽ ´ 3.75-3.97 (4H, m, CH2-CH2), 4.90 (2H, d, J = 17.5 Hz, CH2), 5.44 (2H, d, J = 17.5 Hz, CH2), 7.27-7.37 (4H, m, ArH), 7.41-7.48 (2H, m, ArH), 7.51 (2H, app. d, J = 8.6 Hz, ArH), 7.67 (2H, app. d, J = 8.0 Hz, ArH), 7.82 (2H, d, J = 8.5 Hz, ArH).   13C NMR (100 MHz, CDCl3) ÃŽ ´ 55.2, 55.7, 122.3, 124.4, 126.0, 127.3, 127.5, 128.3, 128.6, 131.5, 132.5, 148.5 ppm.   FTIR 828 (s), 927 (s), 1137 (m), 1209 (m), 1469 (m), 2360 (m), 2900 (m), 2959 (m) cm-1.   Anal. Calcd for C24H20N2:   C 85.68; H 5.99; N 8.33.   Found C 85.73; H 5.68; N 8.59%. 3.3.72,8-Dimethanol-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X(MHK 04-50)The spectrum is terrible there is NO way you can claim to have made this compound see me Starting with 2,8-dimethanol TrÓ §gers base X (400 mg, 1.42 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane: ethyl acetate 1:1) to afford X (134 mg, 32%) as a colourless solid.   m.p. X-Y  °C (lit.ref A-B  °C).2   1H NMR (400 MHz, CDCl3) ÃŽ ´ 1.76 (2H, br s, OH), 3.46-3.64 (4H, m, CH2-CH2), 4.43 (2H, d, J = 17.3 Hz, CH2), 4.47 (2H, s, CH2OH), 4.56 (2H, d, J = 17.2 Hz, CH2), 6.89 (2H, app. s, ArH), 7.02 (2H, dd, J = 1.5, 8.1 Hz, ArH), 7.07 (2H, d, J = 8.0 Hz, ArH), 7.26 (2H, s, ArH).   13C NMR (100 MHz, CDCl3) ÃŽ ´ 54.6, 59.1, 64.8, 126.1, 127.5, 128.1, 136.7, 137.2, 149.6 ppm.   FTIR 750 (s), 884 (s), 1105 (m), 1195 (m), 1328 (m), 1491 (d), 1622 (s), 1701 (s, C=O), 2852 (m), 2893 (bs), 2946 (m) cm-1.   Anal. Calcd for C18H20N2O2:   C 72.95; H 6.80; N 9.45.   Found C XX; H XX; N XX %.   See me is this compound in the literature(NOT charactrised in letreature)   1.  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã‚  Ã ‚  Ã‚   Ishida, Y.; Ito, H.; Mori, D.; Saigo, K., Tetrahedron Lett. 2005, 46, 109-112. 3.3.82-Bromo-8-methyl-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X(MHK-05-18)ACT checked NMR Starting with 2-bromo-8-methyl TrÓ §gers base X (1.30 g, 4.12 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane) to afford X (1.00 g, 73%) as an off-white solid.   m.p. 209-212  °C.   1H NMR (400 MHz, CDCl3) ÃŽ ´ 2.19 (3H, s, CH3), 3.47-3.62 (4H, m, CH2-CH2), 4.37 (2H, app. d, J = 17.1 Hz, CH2), 4.53 (1H, d, J = 17.2 Hz, CH2), 4.54 (1H, d, J = 17.2 Hz, CH2), 6.71 (1H, app. s, ArH), 6.86-6.91 (1H, m, ArH), 6.97 (1H, d, J = 8.3 Hz, ArH), 6.99 (1H, d, J = 7.9 Hz, ArH), 7.03 (1H, d, J = 2.1 Hz, ArH), 7.15 (1H, dd, J = 2.1, 8.3 Hz, ArH).   13C NMR (100 MHz, CDCl3) ÃŽ ´ 20.7, 54.70, 54.74, 58.7, 59.0, 117.5, 127.7, 128.1, 129.1, 129.7, 130.1, 131.4, 134.4, 136.0, 139.2, 147.2, 149.5 ppm.   FTIR 863 (s), 944 (m), 1090 (m), 1219 (s), 1341 (s), 1476 (s), 1518 (s), 2901 (m), 2954 (m) cm-1.   Anal. Calcd for C17H17BrN2:   C 62.02; H 5.20; N 8.51.   Found C 62.29; H 5.12; N 8.68%. 3.3.92-Bromo-8-methoxyl-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X(MHK-04-34)ACT checked NMRReplot 13C with expansions of all picked peaks and show ACTMay need to re-run 13C with more scans not sure about some peaks Starting with 2-bromo-8-methoxy TrÓ §gers base X (500 mg, 1.51 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane:ethyl acetate 2:1) to afford X (180 mg, 35%) as a pale brown solid.   m.p. 156-157  °C.   1H NMR (400 MHz, CDCl3) 3.50-3.60 (4H, m, CH2-CH2), 3.68 (3H, s, OCH3), 4.34 (1H, d, J = 17.3 Hz, CH2), 4.37 (1H, d, J = 17.2 Hz, CH2), 4.52 (1H, d, J 17.3 Hz, CH2), 4.54 (1H, d, J = 17.2 Hz, CH2), 6.42 (1H, d, J = 2.9 Hz, ArH), 6.63 (1H, dd, J = 2.9, 8.6 Hz, ArH), 6.98 (1H, d, J = 8.4 Hz, ArH), 7.01-7.06 (2H, m, ArH), 7.16 (1H, dd, J = 2.0, 8.4 Hz, ArH).   13C NMR (100 MHz, CDCl3) ÃŽ ´ 54.7, 54.8, 55.2, 58.8, 59.2, 112.8, 113.3, 117.6, 128.8, 129.7, 130.2, 131.5, 137.5, 139.0, 149.4, 156.6, 165.6 ppm.   FTIR 805 (m), 846 (m), 1025 (s), 1066 (s), 1278 (s), 1469 (s), 1487 (m), 1594 (m), 2359 (m), 2900 (m) cm-1.   Anal. Calcd for C17H17BrN2O:   C 59.14; H 4.96; N 8.11.   Found C 59.26; H 4.72; N 8.08%. 3.3.102-Ethoxycarbonyl-4,8-dimethyl-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X(MHK-04-30)ACT checked 1H NMR NEED 13C NMR Starting with 2-ethoxycarbonyl-4,8-dimethyl TrÓ §gers base X (500 mg, 1.55 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane:ethyl acetate 4:1) to afford X (88 mg, 17%) as a pale yellow solid.   m.p. 182-185  °C.   1H NMR (400 MHz, CDCl3) ÃŽ ´ 1.32 (3H, t, J = 7.1 Hz, CH3), 2.17 (3H, s, CH3), 2.38 (3H, s, CH3), 3.54-3.66 (4H, m, CH2-CH2), 4.20-4.33 (3H, m, CH2), 4.49 (1H, d, J = 17.4 Hz, CH2), 4.50 (1H, d, J = 17.2 Hz, CH2), 4.60 (1H, d, J = 17.2 Hz, CH2), 6.69 (1H, app. s, ArH), 6.85-6.89 (1H, m, ArH), 7.02-7.09 (1H, m, ArH), 7.46 (1H, app. s, ArH), 7.65 (1H, app. s, ArH).   13C NMR (100 MHz, CDCl3) ÃŽ ´ 14.3, 17.8, 20.7, 54.7, 55.4, 55.4, 59.3, 60.6, 126.1, 127.8, 128.1, 129.0, 130.0, 134.3, 135.5, 136.5, 137.0, 147.2, 152.8, 166.5 ppm.   FTIR 776 (s), 833 (s), 905 (m), 1025 (s), 1215 (s), 1293 (s), 1497 (s), 1709 (s, C=O), 2900 (m) cm-1.   Anal. Calcd for C21H24N2O2:   C 74.97; H 7.19; N 8.33.   Found C 74.72; H 7.25; N 8.41 %. 2.3.118-Bromo-2-ethoxycarbonyl-4-methyl-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X (MHK-05-22)ACT checked NMRNeed to re-run 13C with more scans insufficient aryl peakssections of 1H MR should go in thessi with discussion see ACT Starting with 8-bromo-2-ethoxycarbonyl-4-methyl TrÓ §gers base X (5.50 g, 14.21 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane:ethyl acetate 3:1) to afford X (1.70 mg, 30%) as pale yellow solid.   m.p. 196  °C.   1H NMR (400 MHz, CDCl3) ÃŽ ´ 1.33 (3H, t, J = 7.1 Hz, CH3), 2.36 (3H, s, CH3), 3.54-3.64 (4H, m, CH2-CH2), 4.21 (1H, d, J = 17.5 Hz, CH2), 4.24-4.34 (2H, 2 x overlapping q, J = 7.1 Hz, CH2-CH3), 4.47 (1H, d, J = 17.3 Hz, CH2), 4.49 (1H, d, J = 17.4 Hz, CH2), 4.57 (1H, d, J = 17.3 Hz, CH2), 6.97 (1H, d, J = 8.4 Hz, ArH), 7.01 (1H, d, J = 2.2 Hz, ArH), 7.15 (1H, dd, J = 2.2, 8.4 Hz, ArH), 7.44-7.46 (1H, m, ArH), 7.65-7.67 (1H, m, ArH).   13C NMR (100 MHz, CDCl3) ÃŽ ´ 14.3, 17.8, 54.6, 55.0, 55.2, 59.1, 60.7, 117.6, 126.3, 128.0, 129.9, 130.2, 130.3, 131.2, 135.6, 136.6, 139.1, 149.2, 152.3, 166.4 ppm.   FTIR 827 (s), 927 (s), 1023 (m), 1150 (s), 1387 (s), 1412 (m), 11470 (s), 1704 (s, C=O), 2360 (m), 2900 (m) cm -1.   Anal. Calcd for C20H21BrN2O2:   C 59.86; H 5.27; N 6.98.   Found C 59.76; H 5.19; N 7.21%. 3.3.121,4,8-Trimethyl-2-nitro-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X(MHK-02-10)Need 1H and 13C NMR where are these!!! Starting with 1,4,8-trimethyl-2-nitro- TrÓ §gers base Y (500 mg, 1.62 mmol), the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane:ethyl acetate:hexane 4:1:1) to afford X (153 mg, 29%) as a yellow solid.   m.p. 138-141  °C.   1H NMR (400 MHz, CDCl3) ÃŽ ´ 2.20 (6H, s, CH3), 2.36 (3H, s, CH3), 3.54-3.64 (4H, m, CH2-CH2), 4.33 (1H, d, J = 17.5 Hz, CH2), 4.36 (1H, d, J = 17.6, CH2), 4.50 (1H, d, J = 17.5 Hz, CH2), 4.65 (1H, d, J = 17.6 Hz, CH2), 6.75 (1H, app. s, ArH), 6.89 (1H, app.d, J = 7.9 Hz, ArH), 7.01 (1H, d, J = 8.0 Hz, ArH), 7.40 (1H, s, ArH).   13C NMR (100 MHz, CDCl3) ÃŽ ´ 14.7, 17.8, 20.7, 54.1, 54.9, 55.7, 57.2, 124.1, 125.0, 127.9, 128.3, 128.6, 128.8, 134.2, 134.6, 136.5, 136.8, 147.2, 152.4 ppm.   FTIR 819 (m), 1053 (s), 1185 (m), 1280 (s), 1369 (m), 1497 (m), 2359 (m), 2900 (m), 2987 (m) cm-1.   Anal. Calcd for C19H21N3O2:   C 70.57; H 6.55; N 12.99.   Found C 70.52; H 6.28; N 12.69%. 3.3.142,8-Dimethyl-4-nitro-6H,12H-5,11-ethanodibenzo[b,f][1,5]diazocine X(MHK-02-10, MHK04-66 ChromA1)re-run 1H and 13 Spectra Starting with 2,8-dimethyl-4-nitro-Trà ¶gers base X (500 mg, 1.69 mmol) and 1with heating for 5 days,the crude material obtained upon work-up was chromatographed (silica gel, dichloromethane: ethyl acetate 10:1) to afford Y (120 mg, 23%) as a yellow solid.   m.p. 168-170  °C.   1H NMR (400 MHz, CDCl3) ÃŽ ´ 2.20 (3H, s, CH3), 2.21 (3H, s, CH3), 3.42-3.63 (4H, m, CH2-CH2), 4.44 (1H, d, J = 17.6 Hz, CH2), 4.50 (2H, app. s, CH2), 4.62 (1H, d J = 17.6 Hz, CH2), 6.79 (1H, app. s, ArH), 6.87-6.94 (2H, m, ArH), 7.02 (1H, d, J = 8.0 Hz, ArH), 7.11 (1H, app. s, ArH).   13C NMR (100 MHz, CDCl3) ÃŽ ´ 20.5, 20.7, 54.4, 56.0, 58.0, 59.4, 122.0, 127.5, 128.1, 129.4, 132.2, 134.6, 135.4, 136.0, 139.4, 140.8, 146.9, 150.5 ppm.   FTIR 836 (m), 884 (m), 1021 (m), 1171 (s), 1371 (m), 1521 (s), 2910 (m), cm-1.   Anal. Calcd for C18H19N3O2:   C 69.88; H 6.19; N 13.58.   Found C 69.67; H 6.24; N 13.43%. References 1.Hamada, Y.; Mukai, S., Tetrahedron: Asymmetry 1996, 7, 2671-2674. 2.Ishida, Y.; Ito, H.; Mori, D.; Saigo, K., Tetrahedron Lett. 2005, 46, 109-112. 3.Faroughi, M.; Try, A. C.; Turner, P., Acta Crystallogr., Sect. E: Struct. Rep. Online 2008, 64, o458.

Philosophy: “Explain the Differences Between Plato and Aristotle’s View of Reality”.

Plato imagined that there existed an ideal or perfect world beyond our own physical earth. Our earthly world is full of unevenness, imperfections, and impurities which have been copied from the true ideal world which is beyond us. Plato further believed that our physical world and its Forms participate or imitate the real Forms in a disorderly way. He claimed that there was a relationship between the realm of Forms and our world. This relationship revealed to us mortals the forms and brought order to life. Aristotle objected to Plato’s view, arguing that one cannot know the type of interaction which is occurring between the two Forms.If the â€Å"real or ideal forms† are eternal, pure and unchanging then how do they relate to the material objections or Forms on earth with all their physical imperfections? This participation or imitation link between the real and the imaginary (which Plato claimed existed) is erroneous thinking as no one can/has established such a link à ¢â‚¬â€œ real or otherwise. And even if a link is established it fails to explain all the Forms in the material world. At some point Plato fails to explain how this greater Form was controlled- how can Form control things?Was there energy in â€Å"Forms†? Aristotle’s assumption of the Theory of Forms was intimately integrated with his belief that we develop some type of biological and scientific wisdom of a primary substance (be it plant, animal, rock, etc) only when we know what are usually called its â€Å"causes. † The Greek word, aitia, which is translated as â€Å"causes,† is probably better rendered as â€Å"that which explains. † What that means is that our knowledge of something only occurs once we have ascertained why the â€Å"thing† is there and what its uses are (the primitive scientific method).Thus, if the essence of being a humanoid includes being a biped, we are able to explain our two legs by appeal to the form of humanness w hich is in us. So knowledge of the form or essence is in effect knowledge of the thing’s causes, of what explains why it is what it is. In this way Aristotle’s theory of knowledge was integrated with his metaphysics or scientific method. Thus, if the essence of being a humanoid includes being a biped, we are able to explain our two legs by appeal to the form of humanness which is in us. So knowledge of the form or essence is in effect knowledge of the thing’s causes, of what explains why it is what it is.In this way Aristotle’s theory of knowledge was integrated with his metaphysics or scientific method. Plato postulated that once the humans rose above their physical environment, they would understand the Forms which were present in the invisible world. Whether he meant this would occur after death or during life remains a mystery. Aristotle on the other hand believed that everything was right here on earth and one could find the Form if one developed a s cientific method to apprehend it . I believe the Forms which Plato believed in were not real.He claims that what we see on earth are mimics of the real thing, only with a lot of imperfections. In his Allegory of the Cave, outlined in The Republic, he called mimics artificial replicas of the real thing. In real life all that is seen is an illusion (smoke) of the real thing. On the other hand, Aristotle believed that our natural world itself was real and physical. Aristotle, having studied some biological and physical phenomenon during his work as a teacher, came to understand that our world was made up of many natural Forms, even though not all of the Forms were ideal, pure or perfect.He argued that with our sense(s) we could identify all the natural Forms on earth. The big question which Aristotle and everyone else asked about Plato’s theory of Forms was ‘what are the two separate realms and what do they mean and how do they explain life as it is? ’ No matter how one analyses Plato’s theory, I would argue it simply fails to explain our physical world, its evolution and the order of things. Why some things are permanent remains a central question in his philosophy. How was the knowledge about our own world derived from the â€Å"ideal Forms†?One can understand that genetic traits can be passed on to future generations of humans and animals, but how does this information pass on to inanimate objects like the stone, rock, sand or water? How could these physical properties with no â€Å"Brain† understand the ideal world? I can understand that perhaps some humans may have ESP and perceive (with a lot of good luck) the past or the future, but how can a rock know that it was a rock in the ideal world first and now is a manifestation of the rock in our world?

Catcher Rye What Is The Hardest Part Of Growing Up

Maddie Malakoff Ms.Reid P.5 September 20, 2017 Catcher in the Rye: What is the hardest part of growing up? The hardest part of growing up is having to make tough decisions in the moment. Not knowing if they are right or wrong, but having to use your best judgment. Those wrong choices give you chance to learn and grow from them, while the right choices set you on a more successful path in the long run. For someone it’s easier to access situations for others they are lost. In the novel Catcher in the Rye by J.D Salinger the main Character Holden Caulfield, a boy from a rich family who is constantly flunking schools and making bad life decisions, like getting into fights and sheltering his feelings from his only friends goes on a†¦show more content†¦Having no role adult role models in his life besides his teachers, he looks to his peers and adopts some of their habits and strategies they use to in tough situations. Since starting off the book we learn that Holden is flunking out of the school he is attending current ly (Pencey Prep) and he is planning to leave before the date he is supposed to and take a trip to New York. Right away this is a coming way out of left field because usually, teenagers don’t go into the city for a few days unaccompanied. Before he left the school he got in a huge fight with his roommate, he kept egging him on calling him names and such and wouldn’t stop even when his roommate asked nicely, he got punched but Stradlater (roommate) instantly felt remorse and said â€Å" Why the hell don’tcha shut up when I tellya to?†(pg58) He didn’t want to hurt Holden but felt like he had no other choice than to hit him, and when he felt bad about it, Holden had a blank expression on his face not even considering that he was also at fault. This happens another time in the book when the prostitute and her pimp come back to Holden s hotel room and he opens his mouth up and gets beaten up once again. Holden said â€Å" You’re a dirty moron, Yo u’re a stupid chiseling moron†¦ and you’ll be---† (p135). He was cut off, punched, and knocked out, his wallet and the money he â€Å"owed† they took, and instead of admitting to himself that he made a mistake and gotten himself in a bad situation heShow MoreRelatedAnalysis Of Salinger s The Catcher s The Rye 2525 Words   |  11 PagesThe Catcher in the Rye (1951) by J.D Salinger is a book with a truly controversial history by being banned from bookstores, libraries, etc. during the time of its release and even now is very scarcely being brought back into the high school setting to be taught as part of the high school curriculum. While being confronted about reasons for being banned, protesters of this book give very vague arguments on why it should be banned such as â€Å"its a very filthy book,† or â€Å"its explicitly pornographic.†Read MoreAnalysis Of The Book The Catcher Of The Rye By Quot. Salinger1240 Words   |  5 Pages The Catcher in the Rye, a novel written by J.D. Salinger, follows the short journey in which a teenage boy is coming to terms with his encroaching adulthood. Holden, the main character, has been kicked out of a private school for the third time. In New York, he is on the verge of a mental breakdown. Holden is reluctant to act on the obvious solution of returning home and feels discombobulation towards the consequences he might have to face. He reflects on the death of his brother and strugglesRead MoreTeenage Years Are Best Years in Ones Life3615 Words   |  15 Pagesteenage years are still nevertheless the best years of ones life. With extra guidance and stricter censorship of metal bands, I believe that the true beauty of teenage years will soon dawn upon the youths in todays society. The Teenage Years Growing up is a hard process, especially for those who are experiencing their adolescent years.    Everyone who has gone through this process agrees that these years have been some of the most awkward and strangest years of their lives; the ‘teen years’ is

Coral Divers Resort Case Solution Essay - 1879 Words

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This solution manages to post a positive profit in the first year of implementation (Displayed in Exhibit 3). However, this alternative does not provide a sustainable revenue stream into the future because the lack of competitive advantage it builds and the intense competition of other shark diving focused resorts in the area (See decreasing profits from years 2010 to 2011 in Exhibit 3). Comparison of Solutions: When it comes to judging the alternatives with the most important factors of profit maximization and competitive advantage, the recommended option to become focused on family diving vacations is much stronger than the option to specialize in shark diving. (Displayed in detail in Exhibit 2). Partnering with Rascals posts the highest first full year profits of $166,000 compared to the adventure focused and cost efficiency alternative that posts a first year profit of $112,000. 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