JEE(ADVANCED) – 2014 PAPER-1 Code-1 Questions with Answers PART – 1 PHYSICS SECTION – 1 (One or More Than One Options Correct Type) This section contains 10 multiple choice type questions. Each question has four choices (A)‚ (B)‚ (C) and (D) out of which ONE or MORE THAN ONE are correct. At time ?? = 0‚ terminal A in the circuit shown in the figure is connected to B by a keyand an (????)‚ with ??0 = 1Aand ω = 500 rad s-1 starts flowing in it with alternating current ??(??) = ??0 cos 1. the
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of malonic acid. The ion reacted with bromobutane which was also in the reaction solution to give the product. The yield product was a butyl derivative of malonic ester that was isolated by adding water to the reaction solution‚ and extracting with ether. The ether was dried and evaporated to give the product. Procedures: 0.039g of tricaprylmethylammonium chloride‚ 0.358g of 1-bromobutane‚ 0.416g ofdiethyl malnote‚ and 0.414g of potassium carbonate were mixed in a 5mL long-necked‚ round-bottom flask
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Chapter 17—Alcohols and Phenols SHORT ANSWER Drawing Instructions: Draw structures corresponding to each of the given names. 1. Draw: cis-4-tert-butylcyclohexanol ANS: 2. Draw: 3-methyl-2-buten-1-ol ANS: 3. Draw: 2-phenyl-2-propanol ANS: 4. Draw: glycerol ANS: 5. Draw: 2‚ 4‚ 6-trinitrophenol ANS: IUPAC Naming Instructions: Provide proper IUPAC names. 6. Name: ANS: (E)-2-ethylbut-2-en-1-ol 7. Name: HOCH2CH2OH ANS:
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UNIVERSITI TEKNOLOGI MARA COURSE INFORMATION Confidential Code Course Level Credit Hours Contact Hours : : : : : CHM 556 Organic Chemistry II Degree 4 3 hr (Lecture) 3 hr (Practical) 3 Core CHM 456 Part Course Status Pre-requisite : : : Course Outcomes : Upon completion of this course‚ students should be able to: 1. Determine functional groups present in organic compounds using Infrared Spectroscopy and interpret Nuclear Magnetic Resonance spectra and relate the information to structural
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LEARNING LOG 2: Observe‚ Connect and Reflect on Your Learning PART III – Symmetry in Crystals The most striking examples of symmetry…are crystals. Herman Weyl Period Focus Image Question Your Observations Complete at the end of Week 5 Image 5 Uvarovite is a gemstone rich in chromium. What are your main observations about uvarovite symmetry from studying the external form? (30 - 40 words) (2 marks) What is your personal favourite gemstone and what is its space group. (up to
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Chem 30A Ch.1-4: Condensed Chang’s Class Notes Chapter 1 Valence electrons octet rule exceptions P and S can have 10 or 12 valence e- B and Al (Group 3) can have 6 valence e- electronegativity- how much an atom wants e- < 0.5 = nonpolar‚ covalent (i.e. H2) 0.5 - 1.9 = polar covalent direction of polarity (using arrow and delta symbol) overall dipole > 1.9 = ionic formation of ions fish-hook arrow Lewis structure formal charge Functional Groups Molecular Shape VSEPR (Valence Shell
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Compound Molecular Structure Molecular Weight (g/mol) Melting point (0C) Solubility Hazard Sulfuric acid (H2SO4) 98.079 10 Miscible in water Hazardous in case of eye contact (irritant)‚ of ingestion‚ of inhalation. Slightly hazardous in case of skin contact (irritant) Ammonium Bromide (NH4Br) 97.94 452 Soluble in water Hazardous in case of eye contact (irritant)‚ of ingestion‚ of inhalation. 1-Butanol (C4H10O) 74.12 -89.8 Soluble in water. Very soluble in acetone‚ miscible with ethanol‚
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Alcohol based fuels are used as alternatives to fuels that come entirely from non-renewable resources. The most common of these are ethanol and methanol. These two substances have a few similarities‚ but also significant differences. The similarities are so few that they can be listed concisely; just appearance and smell are similar for these two chemicals. If an individual were presented with samples of each of these chemicals‚ they would have to ignite it or consume it in order to tell the
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38 Sujet : Subject Référence : Reference EUROPEAN REGULATION – REACH Pages Pages CE9 Version : Revision Q Date: 09/12/10 Etabli par : V.NGUYEN Established by Validé par : Approved by C. De Meerschman RÉFÉRENCE NORMATIVE NORMES REFERENCE CHAMPS D’APPLICATION APPLICATION FIELD OBJECTIFS PURPOSE Regulation 1907 / 2006 of the 18th December 2006 All the products European frame for the REACH Regulation WARNING: The user is responsible for checking any
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was briefly warmed to initiate the bromination reaction. Afterwards‚ the RBF was placed in and ice-water bath and 1.0 M Br2 in DCM (6.0 mL‚ 6.25 mmol) was added dropwise while stirring. DCM was removed from the reaction by rotary evaporation. Next‚ tert-butylamine (5.0 mL‚ 47.6 mmol) and 5.0 mL of N-methylpyrrolidinone (NMP) were added to the RBF‚ and the flask was heated in a water bath at 50-60 °C and stirred for 10 minutes. The reaction mixture was transferred to a separatory funnel along with
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