The prescribed procedure produced nylon. The initial indication that nylon was being formed was through the combination of 0.02M of sebacoyl chloride in hexane and 0.05 M 1‚6 hexanediamine. Due to the fact there was an evident product formed after the combination of these two solutions‚ this simply shows that nylon was produced. The prescribed procedure produced nylon due to the fact that there was a present product of the reaction within the IR spectrum. The main peaks of frequency for the unknown
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1 CHM 1321 Second Midterm Apr 1 – 2011 (Prof. S. Gambarotta) Your Name: ___________________ Student #: ______________ Exercise key Exercise key 1
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1 Haloalkanes and Haloarenes IIT-JEE Chemistry Siddhivinayaka Educational Academy Rajendra Nagar Chowk Link Road Bilaspur Ph-07752- 237799/238799 Website : www.bajpaigroup.com. e-mail - info@bajpaigroup.com CHAPTER 23 LEARNINg OBJECTIvES (i) Name haloalkanes and haloarenes according to the IUPAC system of nomenclature from their given structures. (ii) Describe the reactions involved in the preparation of haloalkanes and haloarenes and understand various reactions that they undergo.
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How to Think Like a Computer Scientist: Learning with Python 3 Documentation Release 3rd Edition Peter Wentworth‚ Jeffrey Elkner‚ Allen B. Downey and Chris Meyers August 12‚ 2012 CONTENTS 1 2 3 The way of the program 1.1 The Python programming language 1.2 What is a program? . . . . . . . . . 1.3 What is debugging? . . . . . . . . 1.4 Syntax errors . . . . . . . . . . . . 1.5 Runtime errors . . . . . . . . . . . 1.6 Semantic errors . . . . . . . . . . . 1.7 Experimental debugging . . .
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SONUBHAU BASWANT COLLEGE OF ARTS‚ COMMERCE & BSc.IT. µCERTIFICATEµ This is certify that‚ ‘GROUP’ has completed the report entitled “LIBRARY MANAGEMENT SYSTEM” As a part of their partial fulfillment for the subject “presentation & communication technique” of Second year B.Sc.IT during academic year 2009 – 2010. Group members are as follows. HEAD OF DEPT. PRINCIPAL PROFESSOR ACKNOWLEDGEME NT The enduring pages of the work are the cumulative sequence of extensive guidance and arduous work. I
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Introduction Friedel-Crafts acylation of anisole with acetic anhydride was used in this experiement to synthesize 4-methoxyacetophenone with the use of a reflux apparatus. Friedel-Crafts reactions can be done by alkylation‚ which involves mixing an alkyl or acyl halide with a Lewis acid‚ or acylation‚ which is done with acid chlorides or anhydrides(Lefevre). Acylation was used because it does not have as many disadvantages aklyations reactions have such as polyalkylation‚ second electrophilic attacks
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UNIVERSITY OF SAN CARLOS DEPARTMENT OF CHEMISTRY NAME: Maniwang‚ Ma. Aiza C. DATE: March 21‚ 2011 COURSE: BS Chemistry II APPROVED: ___________ PREPARATION OF AZO DYES ABSTRACT In this experiment‚ the azo dyes p-nitrobenzene azoresorcinol and methyl orange were prepared by the azo coupling reaction. The p-nitrobenzene azoresorcinol dye was prepared from p-nitroaniline and resorcinol. The diazonium salt formed was from the reaction of the cold solution of dissolved p-nitroaniline
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Barry Allahyar Dr. Dodd CHEM 2122 2010-09-16 Experiment 19: Fischer Esterification‚ Conclusion The objective in this experiment was to efficiently perform an Fischer esterification of 1-butanol and acetic acid to form water and n-butyl acetate‚ and to confirm the esterification using IR spectroscopy analysis. It was found that 0.734 grams of n-butyl acetate was formed with a percent yield of 61%. The product was confirmed using IR spectroscopy and boiling point confirmation. The reaction mechanism
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Notes Aldehydes and Ketones The major similarity between an aldehyde and a ketone is the carbonyl group. A carbonyl group is a carbon atom doubly bonded to an oxygen atom. [pic] Both molecules have a carbonyl group‚ the difference the number of carbons bonded to the carbonyl carbon. An aldehyde will have none or one and a ketone will have two carbons. All aldehydes‚ except formaldehyde‚ will have a hydrogen atom on one side of the carbonyl carbon and at least on carbon on the other side
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Results and Discussion: A reaction involving two bond formation was employed for the preparation of 3‚5-disubstituted 1‚2‚4-triazole as nucleobase analog. The hydrazides 2a‚b were allowed to react with the heteroaryl substituted acetonitrile derivatives 1a-c using catalytic amount of K2CO3 and n-butanol as a solvent to afford the disubstituted 1‚2‚4-triazoles 3-7 bearing benzothiazole‚ benzotriazole‚ quinoloxymethyl and benziimidazole ring systems in moderate yields. The structures of compounds
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