Australian Latest Mining Boom Essay Example | Topics and Well Written Essays - 2500 words

Australian Latest Mining Boom - Essay Example Both quantitative and secondary research is done to reach at a conclusion. Contents Topic Page Number 1) Introduction 3-4 2) Main Body a) Fiscal policy challenges emerging out 4-5 of the recent mining boom in Australia b) Resource Rent Taxation and Negative externality 5 c) Economic Framework of Non-Renewable 6 Resource Taxation d) Economic Costs and Benefits of Mining Super 6-8 Profit Tax e) Conclusion 9 f) Recommendations 9 g) Appendix 11 Introduction Mining boom in Australia is an outcome of huge demands for these resources in the global market, mainly Asia because of its growing need for these minerals. In all parts of Australia, mining companies are increasing their present operations, shuttered mines are being re-opened and all this is taking place at a never before pace. Moreover, this latest boom in this mining sector can also be attributed to the expansion in demand for Australian commodities by the foreign nations. This, coupled with decreasing import prices has resulted in an amazing enhancement in their terms of trade. (Banks, 2011, p. 1) At first it was perceived by most of the Australians that the boom in their mining sector had bought unequivocal benefits to their nation’s economy by creating more jobs, generating higher revenues from exports, taxation and higher incomes for most of the people. But studies have revealed that some of these increased profits from the mining companies are at the cost of profits from the non mining institutes (Richardson, 2009, p. 2). Australia is known to be an inherently resource rich nation and one of the leading countries in the world from the point of view of production of minerals. Australia, as already said, is a major exporter of mineral resources, exporting huge amounts to Asia and the Pacific regions. The Australian economy, during 2007 had grown at a rate of 3.9% owing to the increasing global demand for mineral commodities. Since, higher prices in world market for mineral commodities were expected in future as well, the Australian economy kept on expanding. As a result of an increase in the domestic demand for more workers and thinning labor market, in 2007, the consumer price index (CPI) rose by 4.2% (Australia Mineral and Mining Sector Investment and Business Guide, 2006, p. 45). With this boom came the need to review the ongoing tax system in the country. Under the Henry tax reviews the mining super profit tax was introduced which was instantly subjected to a lot of opposition from the mining community as well as the media. Here, in this report, the economic costs and benefits arising out of the mining super profit tax are analyzed and the discussion also includes some reasons as to why this tax is a good/bad policy measure. In this paper, both quantitative and qualitative research has been done. In order to analyze the costs and benefits of the super profit tax, vast literature in the form of journals, articles, books etc. have been reviewed. The proposals made by the gov ernment regarding the use of the revenues that would be generating out of this tax led to the cost-benefit analysis part. Quantitative analysis has been performed to see the amount of revenue that would have generated out of this tax, had it been implemented. Fiscal policy challenges emerging out of the recent mining boom in Australia In the upcoming years, with the increase in value of Australia’

Registerd nurse interview analysis Essay Example | Topics and Well Written Essays - 250 words

Registerd nurse interview analysis - Essay Example She said that this was tough when her children were still young because they rarely see each other due to her schedule. Sometimes, she cannot be with them on holidays because of her work. She said that she does not regard patients as difficult. Sometimes they can be demanding and grumpy but as a nurse, she has to understand the situation of the patient that they just want to feel better. The resource person narrated that nursing is not just an eight to five job where you punch in and get paid. It is a profession as well as a vocation because the job affects people’s lives. To be successful in this profession, one has to be genuinely concerned with people. A nurse has to understand that patients are already in pain and the least the nurse can do is to alleviate and make the pain bearable to the patient. Nurses also work long hours and they do not follow the Monday to Friday work routine nor the eight to five schedule. It is because illness do not follow schedule and hospitals are open throughout the year. There are also emergency cases where a nurse has to work

A Customer who Has Language Barrier that Someone Has Trouble Understan Essay

A Customer who Has Language Barrier that Someone Has Trouble Understanding English - Essay Example This would forge loyal following among its customers who are foreign speakers many of which are big spenders. Customer service can also be easily facilitated if reps can understand the language of the customer. For the customers, this would be a wonderful experience for them to be truly understood by the store where they make their purchases. This would surely develop a strong following among the foreign segment of the market. 3. Include cultural sensitivity training to front liners. There is a significant portion of Macy’s customers who are of foreign origin like me. This would tremendously improve their customer interaction and ultimately customer satisfaction leading to repeat and loyal customers. This would also separate Macy’s from the competition is a more customer-oriented retail store. Macy would also have the benefit of widening its customer base to include foreigners and international students like me. Describe insights you gained by carrying out this ‘shopping trip’ under the consumer role you adopted. What occurred to you that you’ve never thought about before? How do these insights affect the way you think about consumer behaviors and serving consumer markets? Besides the shopper with the specific situation you were assigned, who else might benefit from changes to a store that would better accommodate that kind of shopper? This trip made me realized that customer service is, in fact, a science that retail stores spend time, money and effort to become good at. Reflecting on it, I understand why because if the product and price are the same or even slightly higher, I would tend to buy at the store where I was taken good cared of or had the better customer experience. The store would also benefit from this experience as customers become more conscious of their shopping experience and are likely to provide feedback which could help them improve their products and service.

Executive summary Essay Example for Free

Executive summary Essay Donald, you provided a thorough discussion of what an executive summary really is. Your method of presentation of examples that are equivalent to an executive summary such as a business report or a one-verse summary from the Bible serves as a superb way for the reader to totally appreciate what you are talking about (Marydee, 2004). You also provide the technical features of an executive summary, such as the general length and the scope of such documents (Penrose et al. , 2004). However, I would also want to comment on the tone of your discussion. In your fourth and sixth paragraphs, I noticed that there were a couple of sentences that project a negative attitude among the readers of executive summaries. You mentioned in the fourth paragraph that â€Å"†¦executive summaries are designed for audiences that lack time or motivation to read the full report (Bovee et al. , 2003). † I suggest that you modify this sentence because this connotation of this phrase is not very pleasant for the reader. In the sixth paragraph, you stated, â€Å"†¦most executives habitually make quick decisions, well written executive summaries are arguably the most important information in the business report. † This phrase of yours provides an impression that executives either are not interested in reading the full report, making these individuals not as energetic as they are perceived, or that executives are very gullible because their major decisions are all based on the executive summary. The problem here with your description is that if there is a substandard executive summary that has been generated by a fresh writer, any decisions that will be made by the executive will be significantly influenced by the work produced by this immature writer. I suggest that you incorporate my comments and suggestions so that you will have an improved version of your discussion.

Novel Dihydroquinoline Derivatives Facile Synthesis

Novel Dihydroquinoline Derivatives Facile Synthesis Facile synthesis of novel dihydroquinoline-3,3-dicarbonitriles in the presence of glacial aceticacid as catalyst under solvent-free conditions Masoud Nasr-Esfahani* and Elham Kanaani Department of Chemistry, Yasouj University, Yasouj, Iran Abstract A series of novel dihydroquinoline derivatives were synthesized using malononitrile, 2-aminobenzoic acid and benzaldehydes in the presence of a catalytic amount of acetic acid, without the use of any additional co-catalyst, under solvent-free conditions. The reaction is characterized by high efficiency, easy workup, simple purification of the products and availability of catalyst. Keywords: Dihydroquinoline derivatives, Acetic acid, Malononitrile, 2-Aminobenzoic acid, solvent-free Introduction Heterocyclic compounds including nitrogen, have an important role in organic chemistry. Among these compounds, the quinoline derivatives have attracted great attention because of their application in biological and pharmacological fields. They act as antimalarial,[1-3] anti-psychotic,[4] antihypertensive,[5] anti-parasitic,[6] anthelmintic,[7] antitubercular,[8] antiasthmatic,9] antifungals,[10,11] anticancer,[12] anti-inflammatory,[13] anti-HIV,[14] anti-AIDS,[15] and antineoplastic.[16]A few promising compounds with quinoline ring system are shown as 13 compounds (Fig. 1). Furthermore, quinoline derivatives can be used in the synthesis of fungicides, biocides, alkaloids and flavoring agents,[17] as well as these compounds find use in manufacturing a wide variety of food and lake colors. They could generate a sharp green electroluminescence and have the high quantum efficiency of emission in the blue and the green region.[18] Therefore, in regard to these observations and importance of pharmaceutical and biological of these compounds, herein we study the solvent-free synthesis of novel dihydroquinoline derivatives in presence of glacial acetic acid as catalyst. In the context of green chemistry, the development of clean technologies is very important in organic and medicinal chemistry. The use of available and nontoxic catalysts and replacing solution reactions with solvent-free ones are some cases that can help reduction and elimination of harmful effects of chemical reactions.[19] The volatile nature and toxicity of many organic solvents that are widely used for organic reactions have propounded a serious threat to the environment. Therefore, in recent years, the design of solid-state reaction has received much attention from the eco-friendly synthesis viewpoint.   Solvent-free techniques represent several significant synthetic benefits including savings in money, time and products, and simplicity of the experimental procedure and work-up technique. In recent times application of nontoxic catalysts such as glacial acetic acid in chemical reactions has been an area of interest. Acetic acid is an excellent polar protic solvent and can act as a mild and efficient catalyst for the promotion of the organic reactions. Other factors that stimulate the use of acetic acid include the price of catalyst and simplicity of the work-up procedure. In this research, we report the synthesis of 4-oxo-2-aryl-1,2-dihydroquinoline-3,3(4H)-dicarbonitriles, that involves two steps, in presence of glacial acetic acid under solvent-free conditions. AcOH is an efficient, inexpensive and available acid and in recent decades has been recognizing as a mild catalyst in organic synthesis.[20] Results and Discussion In continuation of our studies in the development of the synthetic methodologiesfor the preparing of fine chemicals and heterocyclic compounds of biological importance,[21-25] herein, we were interested in reporting the synthesis of novel dihydroquinoline derivatives in the presence of the glacial acetic acid as a mild and efficient catalyst. This synthesis involves two steps: firstly, 2-(2-aminobenzoyl) malononitrile intermediate (6) was synthesized via the glacial acetic acid-catalyzed reaction of 2-aminobenzoic acid (4) with malononitrile (5) under solvent-free condition. Subsequently, the novel dihydroquinoline derivatives (8)were prepared by addition of benzaldehyde derivatives (7) to the mixture reaction and attack on the intermediate 6 and followed by intermolecular cyclization (Scheme 1, Table 1). The main advantage ofthis reaction that was carried out with AcOH is that the percentage of peripheral products was low and the recrystallization was also much easier. The 1H NMR spectrum of 8b showed a singlet identified as CH (ÃŽÂ ´ = 4.263 ppm), and a signal at ÃŽÂ ´ 7.831 ppm for NH group. The signals appearing in the 7.308-8.197 ppm are assigned for aromatic rings protons. The proton decoupled 13CNMR spectrum of 8b compound exhibited 14 distinct resonances that confirmed the proposed structure. The infrared spectra (IR) of these compounds show NH bonds appearing at 3388-3453 cm-1. The bands found at 2210-2229 cm-1 are attributed to the CN groups. The intense bands appearing at 1695-1700 cm-1 are assigned to carbonyl groups. The peaks in the region of 1025-1350 cm-1 are assigned for à Ã¢â‚¬ ¦ (C-N) stretching vibration. The proposed mechanism in which acetic acid has catalyzed this conversion was depicted in Scheme 3. Initially, the proton of acetic acid activates carbonyl group of 2-aminobenzoic acid (3) to achieve intermediate 9 and thus increases the electrophilicity carbonyl carbon of acid. In the following, nucleophilic addition of intermediate 10 was done by intermediate 9 and following the loss of H2O intermediate 6 was produced. In the next step, with the addition of an aromatic aldehyde to the reaction mixture, the carbonyl group of aldehyde   was activated by acetic acid to give intermediate 11 thus increases the electrophilicity of carbonyl carbon of aldehyde 7 . The reaction proceeds by nucleophilic addition of the amino group of 6 to the activated aldehyde to afford intermediate 12 and following loss of H2O intermediate 13 was produced. Finally, with intermolecular cyclization of intermediate 13 the product 8 was produced (Scheme 2). Conclusions In summary, a novel class of dihydroquinoline derivatives 8 was obtained using 2-aminobenzoic acid, malononitrile and aromatic aldehydes in presence of AcOH as catalyst under solvent-free conditions. These novel compounds as potentially useful compounds with possible biological and pharmaceutical activities can be applied in various fields such as medicinal and agricultural areas. The most important features of this protocol are an inexpensive and available catalyst, simple purification, easy work-up, with the desired products being isolated in excellent yields. Experimental Section Chemicals and reagents were purchased from Merck, Fluka, and Aldrichchemical companiesand were used without further purification. IR spectra were recorded applying a FT-IR JASCO-680 spectrophotometer in KBr with absorptions in cm-1. The 1H NMR (400 MHz) and 13C NMR (100 MHz) spectra were recorded on a Bruker 400 MHz Ultrashield spectrometer in DMSO-d6 solution with TMS as an internal standard. Mass spectra were recorded by the Fisons Trio 1000 (70 ev). All melting points were measured on a Barnstead Electrothermal (BI 9300) apparatus in open capillary tubes and all are uncorrected. The progress of the reaction was monitored by thin layer chromatography (TLC). General procedure for the synthesis of dihydroquinoline derivatives using AcOH Firstly, a mixture of malononitrile 5 (1.0 mmol, 0.06 g), 2-aminobenzoic acid 4 (1.0 mmol, 0.14 g) and glacial acetic acid (o.2 ml), was heated at 80  °C under solvent-free conditions with concomitant stirring for the 6 h (reactions were monitored by TLC). Subsequently, with the formation of intermediate 6, aromatic aldehyde 7 (1.0 mmol) was added to the reaction mixture, and the mixture was stirred under reflux for the suitable time (reactions were monitored by TLC). After completion of the reaction, ethyl acetate was added and the obtained mixture filtered and then washed with water. After that, the obtained crude products were recrystallized in ethyl acetate to afford the pure product in 70-87% yields (table 1). The products were characterized by IR, 1H NMR, 13C NMR and mass spectroscopic methods. 2-(4-nitrophenyl)-4-oxo-1,2-dihydroquinoline-3,3(4H)-dicarbonitrile (8a): Brown solid, Mp: 238-240  °C;IR (KBr, cm-1): 3440, 3165, 2225, 1695, 1509, 1417, 1344, 1203, 1160, 833, 572; 1H NMR (400 MHz, DMSO-d6): 8.39 (t, 2H, J = 7.8 Hz, aromatic CH), 8.30 (d, 1H, J = 7.6 Hz, aromatic CH), 8.15 (t, 2H, J = 7.8 Hz, aromatic CH), 8.07 (s, 1H, NH), 7.91 (t, 1H, J = 8.4 Hz, aromatic CH), 7.69-7.63 (m, 2H, aromatic CH ), 4.62 (s, 1H, CH); 13C NMR (100 MHz, DMSO-d6): 203.81, 162.54, 149.23, 148.75, 138.52, 131.44, 129.52, 126.17, 124.65, 118.15, 116.19, 111.06, 60.24, 56.02; MS (m/z): 318.1[C17H10N4O3]+, 293.1 [C16H11N3O3]+, 246.1 [C16H12N3]+, 234.1 [C16H12NO]+, 184.1 [C11H8N2O]+, 277, 170, 127, 101, 89, 75. Acknowledgements We are grateful to the Yasouj University for supporting this work. SUPPORTING INFORMATION Experimental method, IR, 1H NMR, 13C NMR, Mass and MP for this article can be found via the Supplementary Content section of this articles webpage. Broom, A. D.; Shim, J. L.; Anderson, G. L. J. Org. Chem. 1976, 41, 1095. References Kaur, K.; Jain, M.; Reddy, R. P.; Jain, R. Eur. J. Med. Chem. 2010, 45, 3245-3264. Marella, A.; Tanwar, O. P.; Saha, R.; Ali, M. R.; Srivastava, S.; Akhter, M.; Shaquiquzzaman, M.; Alam, M. M.   Saudi.   Pharm. J. 2013, 21, 1-12. Wang, X. S.; Zhang, M. M.; Jiang, H.; Yao, C. S.; TU, S. J. Tetrahedron 2007, 63, 4439-4449. Li, K.; Li, Y.; Zhou, D.; Fan, Y.; Guo, H.; Ma, T.; Wen, J.; Liu, D.; Zhao, L. Bioorg.   Med. Chem. 2016, 24,1889-1897. Eswaran, S.; Adhikari, A. V.; Chowdhury, I. H.; Pal, N. K.; Thomas, K. D. Eur. J. Med. Chem. 2010, 45, 3374-3383. Ulahannan, R. T.; Panicker, C. Y.; Varghese, H. T.; Musiol, R.; Jampilek, J.; Alsenoy, C. V.; War, J. A.; Srivastave, S. K. Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 2015, 151, 184-197. Ortiz-Cervantes, C.; Flores-Alamo, M.; Garcia, J. J. Tetrahedron lett. 2016, 57, 766-771. Almansour, A. I.; Arumugam, N.; Kumar, R. S.; Menendez, J. C.; Ghabbour, H. A.; Fun, H. K.; Kumar, R. R. Tetrahedron lett. 2015, 56, 6900- 6903. Ghaffari Khaligh, N. Chin. J. Catal. 2014, 35, 474-480. Safaei-Ghomi, J.; Ghasemzadeh, M. A. J. Nanostruct. 2012, 1, 243-248. R. Musiol, J. Jampilek, V. Buchta, L, Silva, H, Niedbala, B. Podeszwa, A. Palka, K. Mejerz- Maniecka, B. Oleksyn, J. Polanski, Antifungal properties of new series of quinoline derivatives, Bioorg. Med. Chem. 2006, 14, 3592- 3598. M. M. Ghorab, F. A. Ragab, H. I. Heiba, R. K. Arafa, E. M. El-Hossary, In vitro anticancer screening and radiosensitizing evaluation of some new quinolines and pyrimido[4,5-b] quinolines bearing a sulfonamide moiety, Eur. J. Med. Chem. 2010, 45, 3677-3684. Ch. Yu, H. Zhang, Ch. Yao, T. Li, B. Qin, J. Lu, D. Wang, One-pot three-component synthesis of benzo[f]thiopyrano[3,4-b]quinolin-11(8H)-one derivatives, J. Heterocycl. Chem. 2014, 51, 702-705. J. H. Peng, R. H. Jia, N. Ma, G. Zhang, F. Y. Wu, A facile and expeditious microwave-assisted synthesis of furo [3,4-b]indeno[2,1-f]quinolin-1-one derivatives via multicomponent reaction, J. Heterocycl. Chem. 2013, 50, 899-902. C. Benard, F. Zouhiri, M. Normand-Bayle, M. Danet, D. Desmaele, H. Leh, J. F. Mouscadet, G. Mbemba, C. M. Thomas, S. Bonnenfant, M. Le Bret, J. dAngelo, Linker-modified quinoline derivatives targeting HIV-1 integrase: synthesis and biological activity, Bioorg. Med. Chem. Lett. 2004, 14, 2473-2476. X. Xu, W. Liu, Zh. Wang, Y. Feng, Y. Yan, X. Zhang, Silver-catalyzed one-step synthesis of multiply substituted quinolines, Tetrahedron Lett. 2016, 57, 226-229. S. P. Shirame, S. Y. Jadhav, R. B. Bhosale,   Design and synthesis of 1,2,3- triazole quinoline analogues via click chemistry approach and their antimicrobial, antioxidant activites, Asian J. Pharm. Clin. Res. 2014, 7, 163-165. Y. T. Tao, E. Balasubramanian, A. Danel, B, Jarosz, P. Tomasik, Sharp green electroluminescence from IH-pyrazolo[3,4,b]quinoline-based light-emitting diodes, Appl. Phys. Lett. 2000, 77, 1575-1577. M. Nasr-Esfahani, M. Montazerozohori, M. Taei, Aluminatesulfunic acid: Novel and recyclable nanocatalyst for efficient synthesis of aminoalkyl naphthols and amidoalkyl naphthols, C. R. Chim. 2016, 19, 986-994. M.   El-Sayed, K. Mahmoud, A. Hilgeroth, Glacial acetic acid as an efficient catalyst for simple synthesis of dindolymethans, Curr. Chem. Lett. 2014, 3, 7-14. M. Nasr-Esfahani, Z. Rafiee, M. Montazerozohori, H. Kashi, A highly efficient magnetic solid acid nanocatalyst for the synthesis of new bulky heterocyclic compounds, RSC Adv. 2016, 6, 47298- 47313. M. Nasr-Esfahani, M. Montazerozohori, M. Aghel-Mirrzaee, H. Kashi, Efficient and green catalytic synthesis of dihydropyrimidinone (thione) derivatives using cobalt nitrate in solvent-free conditions, J. Chil. Chem. Soc. 2014, 1, 2311-2314. M. Nasr-Esfahani, S. J. Hosseini, M. Montazerozohori, R. Mehrabi, H. Nasrabadi, Magnetic Fe3O4 nanoparticles: efficient and recoverable nanocatalyst for the synthesis of polyhydroquinolines and hantzsch 1,4-dihydropyridines under solvent-free conditions, J. Mol. Catal. A: Chem. 2014, 382, 99-105. M. Nasr-Esfahani, T. Abdizadeh, Nanorod vanadatesulfuric acid as a novel, recyclable and heterogeneous catalyst for the one-pot synthesis of tetrahydrobenzopyrans, J. Nanosci. Nanotechnol. 2013, 13, 5004- 5001. M. Nasr-Esfahani, S. J. Hosseini, F. Mohammadi, Fe3o4 nanoparticles as an efficient and magnetically recoverable catalyst for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones under solvent-free conditions , Chin. J. Catal. 2011, 32, 1484-1489. Figure 1: promising compounds with quinoline ring Scheme 1:Synthesis ofdihydroquinoline-3,3-dicarbonitrile derivatives Table 1. Synthesis of 4-oxo-2-aryl-1,2-dihydroquinoline-3,3(4H)-dicarbonitriles using AcOH Entry R Product Time 1 (h) Time 2 (h) Yield (%) a Mp ( °C) 8a 4-NO2 6 5 87 238-240 8b 4- Cl 6 6 87 201-204 8c 2,4- Cl2 6 6 84 177-179 8d 4- Br 6 8 74 217-225 8e 4- OMe 6 9 77 206-208 8f 4- Me 6 9 69 140-142 a Isolated yield. Scheme 2: Proposed mechanism for the formation of dihydroquinolines 8.

Latex Products In The Work Pla :: essays research papers

Over the last decade, many employees have developed allergies related to the use of latex. “The employees affected have mainly been found in healthcare, food services and in beauty services.'; As employees in these areas, as well as other areas have learned of the potential risk from the contraction of disease leading to death, caused by the exposure to bodily fluids, they have realized that the use of products to stop the exposure is absolutely essential. This has substantially increased and spread the use of latex products, mainly gloves. “The use of so many is very costly, so many employees turned to third world countries who produce a cheaper, untreated latex, which although it cannot be blamed alone for the development of latex allergies, does contribute to the problem.';   Ã‚  Ã‚  Ã‚  Ã‚  The repeated use of latex in the work place can lead to allergies that affect the worker’s ability to function both at work and at home. “The allergies developed can result in degree from a minor irritation to an anaphylactic shock. Out of the many types of allergic reactions only two types, Type I and Type IV have been observed as being related to latex. Type IV reactions have proved to be a response to additives used by the manufacturer. They are uncomfortable, but not life threatening. This is the opposite of Type I reactions. Type I reactions are caused by an antibody called IgE which recognizes the cause of the allergy from previous exposure.';   Ã‚  Ã‚  Ã‚  Ã‚  “The Type I allergens in latex products exist naturally. They remain in the latex during processing. Three proteins found to be involved with the latex allergies are Kd-14, Kd-20 and Kd-27. The proteins can be airborne through powder residue on the gloves, so they can be transmitted through the air. The proteins are also water-soluble. The reactions from Type I include eye, nose, and respiratory symptoms. If left untreated the reaction may be life threatening.';   Ã‚  Ã‚  Ã‚  Ã‚  “The death count associated with Type I reactions up until 1995 is 16 due to latex.'; These deaths prove that the latex allergies that are being developed are a serious risk to employee health, and the matter needs to be dealt with seriously. Both employers and government need to take charge of the issue to ensure the safety of the employees.   Ã‚  Ã‚  Ã‚  Ã‚  The employer needs to provide policies and procedures to reduce the exposure to latex. Until recently latex gloves were the automatic protection worn by all employees dealing with people, or products for people, and in many places this is still the case.

Nutrition Essay -- Health Nutrition Pyramid Diet

Nutrition Paper   Ã‚  Ã‚  Ã‚  Ã‚  When I first began this project I thought the 7 day eating log was going to be a waste of time, but now that have completed it I realize that it is actually very beneficial. I never realized how bad I was eating until I took a step back and looked at it. This has greatly impacted me to change my eating habits, and start to chose healthier foods. Something I learned about myself is that I have a lack of will power when it comes to certain types of candy or food. I saw ice cream come up more than once on the list, which isn’t very healthy. I think this will affect my lifestyle by opening my eyes to my problems with eating, and now I need to correct them.   Ã‚  Ã‚  Ã‚  Ã‚  The movie Super Size Me has been a movie that I have been int...