...on the internet as a student is very important and many students use this information for papers or other assignments. Without the ability of identifying credible a student runs the risk of basing an assignment around information that is misguided, disproven, or flat out untrue. This is why students should learn how to not only gather information but also evaluate it for accuracy and credibility. * * Describe three strategies that students can use to identify which search results are worth exploring when using the Internet to research a topic? There are quite a few strategies students can use to identify which search results are worth exploring. Firstly, looking at the URL is the most important strategy to me. Looking for ".org", ".gov", or ".edu" in the URL is very important. The website name is also important when doing research, remembering that sites like Wikipedia are not as credible as TheNationalGeographic.com, for example. Most things ending in “.com” may not be the most credible in all cases but there are a few. That is why you must also check the summary or description of the search results. Looking at the synopsis and examining the related searches listed is very important. The summary may show signs of bias, which can show whether the site is personal, political, or research oriented. At times the synopsis may be vague but this does not mean the search is...
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...Global strategy of LG Electronics as a leading Korean company Tomikazu Hiraga Senior research Fellow NLI Research Institute Economic recovery in advanced countries including Japan is still sluggish, although corporate financial performance has been recovering gradually. And companies whose business activities in emerging countries experiencing an economic boom account for a larger proportion tend to show better financial performance. Leading Korean companies have a larger presence in the world market and attract considerable attention. I will focus on LG Electronics, Inc., a leading company ranking with Samsung Electronics Co., Ltd. in the world’s electrical and electronics industries, with the largest market share in home appliances markets in important emerging countries, such as India, Brazil, and Indonesia, and relatively advanced management methods including corporate governance, which are highly valued, and will discuss features or important points of its global management and personnel strategy in this article. (Reference: Exchange rates as of August 5, 2010 were as follows. The Japanese yen/Korean won foreign exchange rate was approximately ¥0.074 to the Korean won. The Japanese yen/Indian rupee rate was approximately ¥1.87 to the Indian rupee. ) Leading Korean zaibatsu—The LG group The Korean zaibatsu (chaebol), a unique large companies group, is very influential in Korea’s corporate sector. Top 28 companies by market capitalization other than public corporations account...
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...Global strategy of LG Electronics as a leading Korean company Tomikazu Hiraga Senior research Fellow NLI Research Institute Economic recovery in advanced countries including Japan is still sluggish, although corporate financial performance has been recovering gradually. And companies whose business activities in emerging countries experiencing an economic boom account for a larger proportion tend to show better financial performance. Leading Korean companies have a larger presence in the world market and attract considerable attention. I will focus on LG Electronics, Inc., a leading company ranking with Samsung Electronics Co., Ltd. in the world’s electrical and electronics industries, with the largest market share in home appliances markets in important emerging countries, such as India, Brazil, and Indonesia, and relatively advanced management methods including corporate governance, which are highly valued, and will discuss features or important points of its global management and personnel strategy in this article. (Reference: Exchange rates as of August 5, 2010 were as follows. The Japanese yen/Korean won foreign exchange rate was approximately ¥0.074 to the Korean won. The Japanese yen/Indian rupee rate was approximately ¥1.87 to the Indian rupee. ) Leading Korean zaibatsu—The LG group The Korean zaibatsu (chaebol), a unique large companies group, is very influential in Korea’s corporate sector. Top 28 companies by market capitalization other than public corporations account...
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...LG targets to improve market share in home entertainment segment Published on: April 26, 2011 - 23:46 More in: * Business MUMBAI: Buoyed by surging income levels in the country, Korean consumer durables manufacturer, LG Electronics, is eyeing a 32 per cent market share in home entertainment products and Rs 20,000-crore revenue (from India) by end-this year. “Presently, we have a 29 per cent market share in home entertainment products in India and expect to up it to 32 per cent by December 2011,” LG Electronics India’s managing director, Mr Soon Kwon, told PTI here. “We are targeting around Rs20,000-crore revenue by end-2011 as against Rs 16,000-crore last year. We are growing fast in India and will continue to grow in the market,” he said. LG Electronics India has nine products in the segment and plans to launch more models in this segment in the coming days. “India is one of our key markets. Every year, we are launching some (new) models of home entertainment products in India. We will continue to launch more models in the coming days,” he said. Around 20 per cent of the company’s revenue comes from rural India and it plans to increase this by beefing-up its distribution by opening more outlets, he said. Presently, the company has 20,000 outlets pan-India. LG Electronics competes with Samsung, Philips and Whirlpool in the domestic market. India contributes 6 per cent to the company’s global revenue, he said, adding, “we expect it to double to 12 per cent in...
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...1.0 Introduction of LG Electronics Inc. LG Electronics Inc. is a South Korea multinational electronics company which is also known as the global leader and technology innovator in consumer electronics. The LG Company was a merger of two Korean companies, Lucky and Goldstar, from which the “LG” abbreviation was derived. (Mariush,2012) The company’s headquarter is located in Yeouido-dong, Seoul and the flagship subsidiary of the LG Group. LG has a global sales of KRW (Korean Won) 54.26 trillion which is equal to USD 49 billion in the year 2011. The company operates its business with four business units: mobile communication, air conditioning & energy solution, home entertainment and home appliance. (LG, 2012) It has 75 subsidiaries operates around the world that design and manufacture its products. LG is the world’s second largest flat screen television-set maker after Samsung Electronics Co. (Lee, 2012) Home Entertainment The LG Electronics which is also known as the top global players in home entertainment produces flat panel displays, audio players, video products, monitors, commercial displays and security systems for the consumers and also the commercial markets. LG is not only focusing on creating full-features devices but it is also emphasizing on following the technology boundaries to improve the products. Mobile Communication LG has committed to provide the best ever user experience to expand the next generation of communication by inventing new technologies...
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...J. Org. Chem. 1985,50, 910-912 910 Scheme H I a H N+ C02Et 7c. d H (CHz),, s 0 Sc, d COzEt 8 ( I c , n = l ; d , n = 2. to pyrazolinones 6a,b together with ylides 5a,b as minor products. Bridged 2-pyrazolin-bones 6a,b, whose structures are supported by 'H and 13C NMR spectroscopy, show two strong infrared absorption bands in the 17001800-cm-' range. The first band (1740 cm-') is assigned to the ester carbonyl while we attribute the second one (1765 cm-' for 6a and 1760 cm-l for 6b) to the amide carbonyl. These abnormal high values for an amide band reveal, in accordance with Bredt's rule, an important inhibition of the N-C=O resonance in these N-bridgehead lactams." On the other hand, ' NMR spectra of the crude maH terials obtained from diesters 4c,d at 390-400 "C showed the characteristic signals of a terminal vinyl group suggesting that an elimination reaction follows or competes with the [1,4] migration. Flash column chromatography of the mixture resulting from the thermolysis of the piperidine derivative 4c afforded besides the pyrazolinone 6c12an isomeric N-alkenyl compound whose spectroscopic datal3support the hydroxy-bpyrazole structure 7c. The analogous elimination product 7d formed in lower yield (15% estimation on the basis of 'H NMR spectra) could not be isolated. Pyrazolinone 6c submitted to flow pyrolysis at 400 O C was recovered unchanged. Thus hydroxy-bpyrazoles 7c,d result from an intramolecular elimination...
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...Introduction The transition metal catalyzed cross-coupling reactions such as Negishi,1 Heck,2 Suzuki-Miyaura,3 Stille,4 Kumada,5 Hiyama,6 and Sonogashira7 are extremely powerful tools for making C−C bonds. These methods have been extensively used in wide range of academic areas including material product synthesis, materials science, medicinal, biological, supramolecular chemistry, catalysis and coordination chemistry. Some of these reactions are also useful in pharmaceutical, agrochemical and fine chemical industries.8 Among these powerful transformations, the Suzuki-Miyaura cross-coupling (Scheme 1) (defined as transition-metal catalyzed cross-coupling between an organoboron compound and an organic halide or pseudo halide) is the most widely applied transition-metal catalyzed C−C bond forming reaction since its discovery in 1979.9 Scheme 1. Suzuki-Miyaura cross-coupling reaction. Suzuki reaction has become the most attractive approach for C−C bond formation due to many reasons. Firstly, the mild reaction conditions and broad functional group tolerance of this transformation. Secondly, the use of organoboron reagents has many advantages such as they are inexpensive, some are thermally stable and inert to water and oxygen, thus easy to handle (industry), they transmetallate with a variety of metal compounds under exceptionally mild reaction conditions, low toxicity, good availability of diverse organoboron reagent and easy separation of boron containing by-products from the reaction...
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...| | | BENZANILIDE | PRODUCT IDENTIFICATION | CAS NO. | 93-98-1 | | EINECS NO. | 202-292-7 | | FORMULA | C6H5NHCOC6H5 | | MOL WT. | 197.24 | | H.S. CODE | | | SMILES | | | TOXICITY | | | SYNONYMS | N-Phenyl Benzamide; N-Phenylbenzoic acid amide; | Benzanilid (German); Benzanilida (Spanish); Benzanilide (French); N-Benzoylaniline; N-Phenylbenzamide | CLASSIFICATION | | PHYSICAL AND CHEMICAL PROPERTIES | PHYSICAL STATE | white to grey crystals | MELTING POINT | 163 C | BOILING POINT | | SPECIFIC GRAVITY | 1.315 | SOLUBILITY IN WATER | Insoluble (soluble in alcohol) | pH | | VAPOR DENSITY | | AUTOIGNITION | | NFPA RATINGS | Health: 1; Flammability: 0; Reactivity: 0 | REFRACTIVE INDEX | | FLASH POINT | 180 C | STABILITY | Stable under ordinary conditions. | GENERAL DESCRIPTION & APPLICATIONS | Amide is a group of organic chemicals with the general formula RCO-NH2 in which a carbon atom is attached to oxygen in solid bond and also attached to an hydroxyl group, where 'R' groups range from hydrogen to various linear and ring structures or a compound with a metal replacing hydrogen in ammonia such as sodium amide, NaNH2. Amides are divided into subclasses according to the number of substituents on nitrogen. The primary amide is formed from by replacement of the carboxylic hydroxyl group by the NH2, amino group. An example is acetamide (acetic acid + amide). Amide is obtained by reaction of an acid...
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...ARTICLES PUBLISHED ONLINE: 15 DECEMBER 2014 | DOI: 10.1038/NCHEM.2131 Copper-catalysed selective hydroamination reactions of alkynes Shi-Liang Shi and Stephen L. Buchwald* The development of selective reactions that utilize easily available and abundant precursors for the efficient synthesis of amines is a long-standing goal of chemical research. Despite the centrality of amines in a number of important research areas, including medicinal chemistry, total synthesis and materials science, a general, selective and step-efficient synthesis of amines is still needed. Here, we describe a set of mild catalytic conditions utilizing a single copper-based catalyst that enables the direct preparation of three distinct and important amine classes (enamines, α-chiral branched alkylamines and linear alkylamines) from readily available alkyne starting materials with high levels of chemo-, regio- and stereoselectivity. This methodology was applied to the asymmetric synthesis of rivastigmine and the formal synthesis of several other pharmaceutical agents, including duloxetine, atomoxetine, fluoxetine and tolterodine. C omplex organic molecules play a crucial role in the study and treatment of disease. The extent to which they can be utilized in these endeavours depends on the efficient and selective chemical methods for their construction1. Amines are widely represented in biologically active natural products and medicines2 (a small selection of which are shown in Fig. 1a). Consequently, the selective...
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...Molecules 2014, 19, 6524-6533; doi:10.3390/molecules19056524 OPEN ACCESS molecules ISSN 1420-3049 www.mdpi.com/journal/molecules Communication A Simple Hydrophilic Palladium(II) Complex as a Highly Efficient Catalyst for Room Temperature Aerobic Suzuki Coupling Reactions in Aqueous Media Mengping Guo 1,2,*, Shiwen Liu 1,2, Xiuling Zhou 1, Meiyun Lv 1, Sanbao Chen 1 and Daoan Xiao 1 1 2 Institue of Coordination Catalysis, College of Chemistry and Bio-Engineering, Yichun University, Yichun 336000, China; E-Mails: liushiwen320721@163.com (S.L.); 13879593114@163.com (X.Z.); lvmeiyun2005@163.com (M.L.); 333csb@163.com (S.C.); xiaodaoan2006@163.com (D.X.) Engineering Center of Jiangxi University for Lithium Energy, Yichun University, Yichun 336000, China * Author to whom correspondence should be addressed; E-Mail: guomengping65@163.com; Tel./Fax: +86-0795-320-0535. Received: 8 April 2014; in revised form: 19 May 2014 / Accepted: 19 May 2014 / Published: 21 May 2014 Abstract: A study on room temperature Suzuki cross-coupling in an aqueous medium was carried out using a simple hydrophilic palladium (II) complex, trans-PdCl2(NH2CH2COOH)2 as catalyst in the presence of K2CO3 in air. This approach with a comparatively inexpensive and hydrophilic catalyst, mild reaction condition and aqueous media exhibits excellent catalytic activity towards the Suzuki coupling of aryl bromides and arylboronic acids, and good yields were obtained in the Suzuki coupling of activated aryl chlorides....
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...Extension and Revision of the von Baeyer System for Naming Polycyclic Compounds (Including Bicyclic Compounds) (IUPAC Recommendations 1999) Synopsis, Preamble, VB-1 to VB-5 Contents of Section Synopsis Preamble VB-1 Definitions and Terminology VB-2 Main Ring VB-3 Naming Hydrocarbon Bicylic Systems VB-4 Numbering of Bicyclic Systems VB-5 Main Bridge References for this Section [pic] Synopsis These recommendations document the von Baeyer system for naming polycyclic ring systems described in Rules A-31, A-32 and B-14 of the Nomenclature of Organic Chemistry, Sections A, B, C, D, E, F and H, 1979 and R-2.4.2 of A Guide to IUPAC Nomenclature of Organic Compounds, 1993 and extend the system to cover more complex cases. It provides guidance on the naming of ring systems which previously the rules did not cover. The method is to identify the main ring and main bridge which provide the basic bicyclic system and to number these atoms. Then all further bridges, whether or not they include additional atoms, are identified by indicating not only the number of atoms but also the two atoms to which the bridge is attached. The final name also indicates the number of rings and the total number of skeletal atoms in the ring system. Heteroatoms, unsaturation and substituents are indicated in the usual way. Preamble This system of naming polycyclic compounds was first developed for bicyclic compounds by von Baeyer (ref 1) and was extended to tricyclic systems by Buchner and Weigand...
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...[4 + 2] cycloaddition reactions have been a valuable research topic for scientists for some time now. More specifically, the combination of dienes and carbonyl containing compounds have been studied primarily for their ability to combine together to form six membered oxygen heterocycles (1). The synthesis of oxygen heterocycles is a valuable tool, as these molecules are precursors to some natural products and they are also components in the synthesis of various carbohydrates (4). The general method utilized to form oxygen heterocycles was to combine an aldehyde as the heterodienophile and a diene in a hetero-Diels-Alder reaction. Extensive studies on this reaction have been completed. Huang and Rawal chose to study this reaction using hydrogen bond promoted ketones as the heterodienophile rather than aldehydes. This is the first time that unactivated ketones have been successfully utilized in a hetero-Diels-Alder reaction. This research is extremely valuable as it expands the extent by which oxygen heterocycles can be formed. This is extremely important to the biological chemists who study and utilize oxygen heterocycles frequently (1). Huang and Rawal began their study by observing the hetero-Diels Alder reaction rates between various aldehydes and the diene 1-amino-3-siloxybuadiene. They found that the reaction rate was siginificantly higher in polar protic solvents rather than polar aprotic solvents (2). They attributed this change in the reaction rate to...
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...Hunter College, CUNY Chem104LC Spring 2015 General Chemistry 2: Spring 2015 Section 01: Tu/Fr, 9:10am - 11:00am Section 02: Sa, 10:10am – 12:00pm Instructors: Sec 01: Nadya Kobko, PhD (Room 1320HN) Sec 02: Ravichandra Bachu, PhD (Room TBA) Email: nkobko@hunter.cuny.edu Email: rbachu@hunter.cuny.edu Office Hours: We 4 to 7 pm (or by appt.) Office Hours: TBA (1403HN, Sa) Goal of the course: This is the second semester of a 2-semester general chemistry sequence that you began in Chem 102 last semester. In Chem 104 we will cover the topics of kinetics, equilibrium, acids and bases, buffers, complex ions, thermodynamics, electrochemistry and nuclear chemistry. Chem 104 is a demanding course (more so than Chem 102) and to achieve success in this course you will need to organize large quantities of information in coherent ways so that you are able to recall and apply your knowledge. In addition you will have to learn to organize your time efficiently. And the mathematics is more demanding than in Chem 102! This semester general chemistry is run using a flipped classroom model. In this model you will watch videos and complete online homework at home and then come to class to complete workshop assignments (during your recitation section) and participate in peer-learning activities using an iClicker (during lecture every Friday). On Tuesdays during lecture we will stream the class videos for the week. This class is an optional component of the course. You should plan to spend at least...
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...A Grignard-Like Organic Reaction The Synthesis of 1-phenyl-3-buten-1-ol Introduction The Grignard reaction is an important synthetic process by which a new carbon to carbon bond is formed. Magnesium metal is first reacted with an organic halide forming the Grignard reagent. The Grignard reaction is the addition of an organomagnesium halide (Grignard reagent) to a ketone or aldehyde, to form a tertiary or secondary alcohol, respectively. For example, the reaction with formaldehyde leads to a primary alcohol. Grignard Reagents are also used in the following important reactions: The addition of an excess of a Grignard reagent to an ester or lactone gives a tertiary alcohol in which two alkyl groups are the same, and the addition of a Grignard reagent to a nitrile produces an unsymmetrical ketone via a metalloimine intermediate. A sample Grignard reaction mechanism can be seen in Figure 1 of a Grignard reagent being prepared with an alkyl bromide and later reacted with a formaldehyde to produce a primary alcohol. The purpose of this lab was to form 1-phenyl-3-buten-1-ol using a Grignard reaction. The Grignard reactant was produced from Zinc and Allyl Bromide which was then reacted to Benzaldehyde. The formation of the final product will be confirmed using a Thin Layer Chromatography, TLC, of the product and Benzaldehyde and an IR analysis of the product. Abstract In reactions involving Grignard reagents, it is important to exclude water and air, which rapidly destroy...
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...SN2 vs. E2 SN2 and E2 reactions share a number of similarities. Both require good leaving groups, and both mechanisms are concerted. SN2 reactions require a good nucleophile and E2 reactions require a strong base. However, a good nucleophile is often a strong base. Since the two reactions share many of the same conditions, they often compete with each other. The outcome of the competition is determined by three factors: the presence of antiperiplanar β -hydrogens, the degree of α and β branching, and the nucleophilicity vs. basicity of the reactant species. In order for an E2 elimination to occur, there must be antiperiplanar β -hydrogens to eliminate. If there are none, the SN2 reaction will dominate. On the same token, the SN2 nucleophile needs a free path to the σ * C-LG antibond. α and β branching block this path and reduce the proportion of SN2 relative to E2 . E2 occurs even with extensive branching because it relies on the β -hydrogens, which are much more accessible than the σ * C-LG antibond. The identity of the nucleophile or base also determines which mechanism is favored. E2 reactions require strong bases. SN2 reactions require good nucleophiles. Therefore a good nucleophile that is a weak base will favor SN2 while a weak nucleophile that is a strong base will favor E2. Bulky nucleophiles have a hard time getting to the α-carbon, and thus increase the proportion of E2 to SN2. Polar, aprotic solvents increase nucleophilicity, and thus increase the rate of SN2. SN2 ...
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