Experiment VIII was performed to analyze SN2 and SN1 using tertiary and primary substrates and use gas chromatography (GC) to examine the SN1 reaction. The product of the SN2 reaction was classified as n-butyl iodide by using infrared spectroscopy and gas chromatography mass spectroscopy and the product of the SN1 reaction was identified as of t-butyl chloride by using infrared spectroscopy and gas chromatography. For the SN2 reaction, 7.62 grams of n-butyl bromide, 20.0 grams of sodium iodide, and 79.1 grams of acetone were used to produce 3.12 grams of n-butyl iodide. The limited reagent was identified as n-butyl bromide and the theoretical yield of n-butyl iodide was calculated as 10.3 grams. The percent yield of this reaction was calculated
Results The lab experiment was done in two parts, one with the NAND, NOR, XOR and Hex Inverters and the other with a 7483 full adder gate, both will verify the truth table when two input bits and a carry are added together. The circuits were built by examining the 1 bits through a K-Map to create a Boolean expression for the sum and carry. The Boolean expression for the sum was A⊕B⊕C and the carry as AB+BC_in+AC_in. From these two expressions, we notice that we must use two exclusive-ORs gates in the sum inputs for A, B, and C. For the sum, we have to use NOR and NAND (the only available gates from the lab manual).
For most sequences at position 4 and 5 we observe only the nucleotides G and T, respectively. There may be rare cases where other nucleotides may also be found. To consider such observations, we need to do a process called additive smoothing or Laplace smoothing to smooth the categorical data. [9] In this case, we add 4 sequences: AAAAAAAAA, CCCCCCCCC, GGGGGGGG, TTTTTTTTT.
Experiment 7 In this experiment we configured several DC circuits consisting of an emf and a network of resistors. The circuits were composed of a power supply, two DMMs, a circuit board, an SPST switch, and an assortment of known resistors along with one unknown resistor. We measured the current and voltage of the entire circuit as well as the potential drops across each resistor to determine the parameters of the circuit including the resistance, voltage, and current for each component.
Figure shows the intersection of line joining the camera center and image points ${\bf x}$ and ${\bf x'}$ which will be the 3D point ${\bf X}$.\\ \end{figure} The ‘gold standard’ reconstruction algorithm minimizes the sum of squared errors between the measured and predicted image positions of the 3D point in all views in which it is visible, i.e.\\ \begin{equation} {\bf X=\textrm{arg min} \sum_{i} ||x_i-\hat{x_i}(P_i,X)||^2} \end{equation} Where ${\bf x_i}$ and ${\bf \hat{x_i}(P_i,X)}$ are the measured and predicted image positions in view $i$ under the assumption that image coordinate measurement noise is Gaussian-distributed, this approach gives the maximum likelihood solution for ${\bf X}$. Hartley and Sturm [3] describe a non-iterative
1. There are two ways of maximizing points in this experiment. The first one is that I should connect myself to a vertex that is in the biggest component and purchases immunization. Since the probability of being infected is based off of expected value, I would have less than 1% chance of getting infected. The second way is that I try to make myself stay in the second-largest connected component.
Introduction An unimolecular substitution reaction, SN1 reaction, has a two step mechanism that results in a halide group being displaced by a nucleophile1. In an SN1 reaction, the first step involves the leaving of a halide group to form a carbocation intermediate. This is the rate determining step, and it is also the slowest step. In the second step a nucleophile attacks a face of the the carbocation. Figure 1 displays this mechanism.
Aims of experiment • Determine the rate constants for hydrolysis of (CH3)3CCl in solvent mixtures of different composition (50/50 V/V isopropanol/water and 40/60 V/V isopropanol/water) • Examine the effect of solvent mixture composition on the rate of hydrolysis of (CH3)3CCl Introduction With t-butyl chloride, (CH3)3CCl, being a tertiary halogenoalkane, it is predicted that (CH3)3CCl reacts with water in a nucleophilic substitution reaction (SN1 mechanism), where Step 1 is the rate-determining step. The reaction proceeds in a manner as shown
The reaction chamber was attached to an Oxygen collection tube. Water is filled at least three-quarters the way up in the bucket. Various percentages of substrate concentration (5%, 15%, and 25%) was added to the reaction chamber and the Oxygen tube is filled with water and contained a water bubble at the top. The initial height of the water in the Oxygen tube was recorded. After 30 seconds, the total change was determined and recorded.
2.4 Band Division and Energy Computation: The power spectrum of the signal is multiplied by magnitude response of set of 33 triangular band pass filters and in the range 300Hz-2000Hz. Sub-bands are formed by using the logarithmic spacing. The positions of these filters are equally spaced along the Mel frequency, which is related to the common linear frequency f by following formula: Mel (f) = 1125* ln (1+f/700) (3) Mel frequency is proportional to the logarithm of linear frequency and which is close to the human perceptual system. 2.5 Sub Fingerprint Generation:
Lab report: How does the surface area affect the rate of reaction ? Introduction The rate of a chemical reaction (or reaction rate) is a calculation of the total time needed for a reaction to take place, or how quickly the reactants are transferred into products in a chemical process. This rate can be measured in two methods. The first one is to measure the rate at which the reactants are used up per unit of time, while the second method is to measure the rate at which the products are formed per unit of time. There are several factors that affect the rate of a reaction.
Experiment 2 Report Scaffold (Substitution Reactions, Purification, and Identification) Purpose/Introduction 1. A Sn2 reaction was conducted; this involved benzyl bromide, sodium hydroxide, an unknown compound and ethanol through reflux technique, mel-temp recordings, recrystallization, and analysis of TLC plates. 2. There was one unknown compound in the reaction that was later discovered after a series of techniques described above.
Title: THE BALLOON INFLATION REACTION Introduction: Chemistry is one thing that makes us understand and gives us reasons of why certain reactions gives certain results. In this experiment we will be illustrating the reaction between baking powder and vinegar and see what happens to the balloon that is attached to it. Hypothetically the reaction of the vinegar and baking powder will produce carbon dioxide which will inflate the balloon. If the more vinegar may happen that when more vinegar is added to the baking powder it may produce more carbon dioxide thus the balloons diameter increases.
It is type of condensation reaction, which involve the condensation of acidic anhydride and aldehyde in the presence of weak base (i.e. Sodium and potassium salt of the acid or trimethylamine) to give unsaturated carboxylic acid.(Equation-1)[1].In 1968 Perkin described the very first example of such type condensation reaction, involve the synthesis of coumarin by condensing the sodium or potassium salt of salicylaldehyde with acetic anhydride (Equation-2)[2].Generally such type of reaction is only applicable to aromatic aldehyde and useful for the preparation of substituted cinnamic acid (Equation-3)[3] Equation-1 Equation-2 Equation-3 In 1883.A very important variation is done by plӧchl, which involve the heating of benzaldehyde
For chlorination SOCl2 used. We have synthesized carboxamide derivatives using NTAA and 3-(3-benzyl-4,5-dihydroisoxazol-5-yl)pyridine and 3-benzyl-5-(3-nitrophenyl)-4,5-dihydroisoxazole by coupling reaction using dichloromethane as a solvent and the product obtained in 1.5-2 hours by stirring only. After synthesis of these carboxamide derivatives , The compounds are characterized by FTIR, 1HNMR, CMR, UV-Visible and mass spectral analysis. The analysis data is in good correlation with structure of
In this experiment, the objective was to synthesize turt-butyl chloride via an sn1 reaction and use sodium iodide and silver nitrate reagents to test the reactivity (book cite). Sn1 stands for first-order nucleophilic substitution (book cite). A substitution reaction is when another atom replaces the halide ion (book cite). The other reaction that can take place is what’s called the elimination reaction. This involves a halide ion leaving with a different atom.