This presentation is all about UV spectroscopy
In this presentation I discussed principle of UV spectroscopy, Absorption law, Intensity shift ,effect of solvent on Absorption shift and all type of transition in UV spectroscopy.
We all know that UV spectroscopy deals with the determination of structure of compounds with interaction of electromagnetic radiation (UV rays) with matter. And i mentioned about principle how UV spectroscopy work in which I discussed about excitation of matter electron and how we used absorption spectra in terms of absorbance.
I also mentioned about effect of solvent on Absorption shift how the polar and non-polar compound are affected when we change the polarity of solvent.
This document discusses chromophores, auxochromes, and spectral shifts in organic chemistry. It defines chromophores as the part of a molecule responsible for its color and absorption spectrum. Auxochromes are substituents that modify a chromophore's absorption by increasing conjugation. There are two types of spectral shifts: bathochromic shifts move absorption to longer wavelengths (red shift) while hypsochromic shifts move it to shorter wavelengths (blue shift). Hyperchromic effects increase absorption intensity while hypochromic effects decrease it. Examples like phenol and nitrobenzene are provided.
This document discusses absorption laws, chromophores, and limitations in ultraviolet-visible spectroscopy. It describes Beer's law and Lambert's law, which state that absorbance is directly proportional to concentration and path length. Deviations from these laws can occur. Chromophores are groups that absorb specific wavelengths, while auxochromes induce bathochromic shifts. Substituents can cause bathochromic, hypsochromic, hyperchromic, or hypochromic shifts in absorption. UV-Vis spectroscopy has many applications in qualitative and quantitative analysis.
The document discusses how solvents and chromophores affect UV-visible spectroscopy. It states that the solvent exerts influence on the absorption spectrum, with the same drug showing different absorption maxima in different solvents. Common solvents used are water, methanol, ethanol, ether, and cyclohexane. The solvent should not absorb in the region studied and have minimum interaction with solute. Chromophores like conjugated systems, carbonyls, and metal complexes determine absorption. Factors like conjugation, auxochromes, and solvent polarity can shift absorption maxima.
This document discusses chromophores and auxochromes in ultraviolet-visible spectroscopy. It defines chromophores as groups that absorb in the UV-visible region and undergo π → π* or n → π* transitions. Examples include ethylenic, carbonyl, and nitrile groups. Auxochromes are groups that shift absorption to longer wavelengths by extending conjugation but do not absorb themselves, such as -OH, -NH2. Bathochromic and hypsochromic shifts change the absorption maximum wavelength while hyperchromic and hypochromic effects alter absorption intensity. Woodward-Fieser rules relate conjugation in dienes to absorption maximum.
UV spectroscopy involves promoting electrons from the ground state to excited states of molecules using ultraviolet radiation between 200-400 nm. Lambert's law, Beer's law, and the Beer-Lambert law describe how the intensity of light decreases exponentially with increasing thickness or concentration of an absorbing substance. Different types of electronic transitions that can occur include sigma-sigma*, n-sigma*, and pi-pi* transitions. Chromophores are functional groups that absorb UV radiation, while auxochromes modify the absorption wavelength or intensity. Bathochromic, hypsochromic, hyperchromic, and hypochromic shifts describe changes in absorption maximum or intensity upon addition of substituents or change of solvent.
UV spectroscopy involves promoting electrons from the ground state to excited states of molecules using ultraviolet radiation between 200-400 nm. The absorption of this radiation can be quantified using Beer's law and plotted in an absorption spectrum showing the wavelength of maximum absorption (λmax) and intensity (εmax). Chromophores are functional groups that absorb UV radiation, while auxochromes modify the absorption by inducing bathochromic, hypsochromic, hyperchromic, or hypochromic shifts.
This presentation is all about UV spectroscopy
In this presentation I discussed principle of UV spectroscopy, Absorption law, Intensity shift ,effect of solvent on Absorption shift and all type of transition in UV spectroscopy.
We all know that UV spectroscopy deals with the determination of structure of compounds with interaction of electromagnetic radiation (UV rays) with matter. And i mentioned about principle how UV spectroscopy work in which I discussed about excitation of matter electron and how we used absorption spectra in terms of absorbance.
I also mentioned about effect of solvent on Absorption shift how the polar and non-polar compound are affected when we change the polarity of solvent.
This document discusses chromophores, auxochromes, and spectral shifts in organic chemistry. It defines chromophores as the part of a molecule responsible for its color and absorption spectrum. Auxochromes are substituents that modify a chromophore's absorption by increasing conjugation. There are two types of spectral shifts: bathochromic shifts move absorption to longer wavelengths (red shift) while hypsochromic shifts move it to shorter wavelengths (blue shift). Hyperchromic effects increase absorption intensity while hypochromic effects decrease it. Examples like phenol and nitrobenzene are provided.
This document discusses absorption laws, chromophores, and limitations in ultraviolet-visible spectroscopy. It describes Beer's law and Lambert's law, which state that absorbance is directly proportional to concentration and path length. Deviations from these laws can occur. Chromophores are groups that absorb specific wavelengths, while auxochromes induce bathochromic shifts. Substituents can cause bathochromic, hypsochromic, hyperchromic, or hypochromic shifts in absorption. UV-Vis spectroscopy has many applications in qualitative and quantitative analysis.
The document discusses how solvents and chromophores affect UV-visible spectroscopy. It states that the solvent exerts influence on the absorption spectrum, with the same drug showing different absorption maxima in different solvents. Common solvents used are water, methanol, ethanol, ether, and cyclohexane. The solvent should not absorb in the region studied and have minimum interaction with solute. Chromophores like conjugated systems, carbonyls, and metal complexes determine absorption. Factors like conjugation, auxochromes, and solvent polarity can shift absorption maxima.
This document discusses chromophores and auxochromes in ultraviolet-visible spectroscopy. It defines chromophores as groups that absorb in the UV-visible region and undergo π → π* or n → π* transitions. Examples include ethylenic, carbonyl, and nitrile groups. Auxochromes are groups that shift absorption to longer wavelengths by extending conjugation but do not absorb themselves, such as -OH, -NH2. Bathochromic and hypsochromic shifts change the absorption maximum wavelength while hyperchromic and hypochromic effects alter absorption intensity. Woodward-Fieser rules relate conjugation in dienes to absorption maximum.
UV spectroscopy involves promoting electrons from the ground state to excited states of molecules using ultraviolet radiation between 200-400 nm. Lambert's law, Beer's law, and the Beer-Lambert law describe how the intensity of light decreases exponentially with increasing thickness or concentration of an absorbing substance. Different types of electronic transitions that can occur include sigma-sigma*, n-sigma*, and pi-pi* transitions. Chromophores are functional groups that absorb UV radiation, while auxochromes modify the absorption wavelength or intensity. Bathochromic, hypsochromic, hyperchromic, and hypochromic shifts describe changes in absorption maximum or intensity upon addition of substituents or change of solvent.
UV spectroscopy involves promoting electrons from the ground state to excited states of molecules using ultraviolet radiation between 200-400 nm. The absorption of this radiation can be quantified using Beer's law and plotted in an absorption spectrum showing the wavelength of maximum absorption (λmax) and intensity (εmax). Chromophores are functional groups that absorb UV radiation, while auxochromes modify the absorption by inducing bathochromic, hypsochromic, hyperchromic, or hypochromic shifts.
There are four main types of shifts that can occur in the absorption maximum of compounds:
1. Bathochromic shift (Red shift) occurs when the absorption maximum shifts to longer wavelengths, such as when multiple chromophores are present in a molecule.
2. Hypsochromic shift (Blue shift) occurs when the absorption maximum shifts to shorter wavelengths, due to removal of conjugation or changes in solvent polarity.
3. Hyperchromic shift increases the intensity of absorption at the same wavelength maximum, often due to the introduction of auxochromes.
4. Hypochromic shift decreases the intensity of absorption, which can result from structural deformations introduced by certain groups.
This document discusses chromophores and how solvents affect absorption spectra. It defines a chromophore as a covalently bonded group that absorbs UV or visible radiation. Chromophores are classified as independent or dependent based on the number needed to impart color. Absorption maxima can shift to longer (bathochromic) or shorter (hypsochromic) wavelengths due to auxochromes or solvent changes. Solvent polarity also affects absorption based on the type of electronic transition involved. Temperature and solvent interactions determine the fineness of absorption bands.
Uv absorption spectra arise from electronic transitions in molecules where electrons move from lower to higher energy levels. The amount of energy absorbed is proportional to the concentration of the solution based on Beer-Lambert's law. Uv-visible spectroscopy can be used to determine structural information about organic compounds, identify additional impurities, and perform quantitative analysis of compounds that absorb uv radiation.
UV-Visible Spectroscopy involves studying the interaction of ultraviolet and visible light with molecules. When light of an appropriate wavelength is absorbed by a molecule, an electron is promoted to a higher energy orbital, exciting the molecule. The wavelength of absorbed light provides information about energy gaps related to functional groups. Absorption follows Beer's law - absorption is proportional to concentration and path length. Molar absorptivity values characterize absorption strength. Chromophores are the parts of molecules that absorb UV-visible light. Conjugation and substituent effects can cause shifts and changes in absorption intensity.
UV-Visible Spectroscopy involves the interaction of electromagnetic radiation in the ultraviolet and visible spectral regions with matter. When molecules absorb this radiation, electrons are excited from one energy level to a higher level. This causes absorption bands to appear in the absorption spectrum. Beer's law states that absorbance is directly proportional to concentration and path length. Chromophores are groups that absorb radiation, while auxochromes shift absorption to longer wavelengths by extending conjugation. Spectroscopy has applications in quantitative analysis, qualitative analysis, detection of functional groups and impurities, and determination of properties like extent of conjugation.
UV-Visible spectroscopy uses electromagnetic radiation to analyze molecular structure by measuring absorption of specific wavelengths. It follows Beer's and Lambert's laws, where absorbance is proportional to concentration. Absorption is due to electronic transitions between orbitals. Deviations from Beer's law can occur at high concentrations or due to chemical changes. Chromophores and auxochromes determine absorption wavelength. Applications include structure elucidation, quantitative analysis, and detection of impurities.
This document discusses ultraviolet-visible spectroscopy and its principles. It covers the electromagnetic spectrum, units used, absorption laws including Lambert's law and Beer's law. It describes chromophores and auxochromes, types of electronic transitions, factors affecting absorption bands, and solvent effects. Different types of absorption bands and applications of UV-Vis spectroscopy are also summarized.
1) The absorption of light by organic compounds involves the promotion of electrons from ground state to excited state molecular orbitals. Sigma electrons undergo σ-σ* transitions at shorter wavelengths while pi and non-bonding electrons undergo π-π* and n-π* transitions at longer wavelengths.
2) Chromophores are functional groups responsible for electronic transitions, imparting color. Auxochromes enhance absorption by chromophores through resonance. Conjugation and pH can shift absorption to longer wavelengths while dilution, solvents, and temperature can affect absorption spectra.
3) Spectrophotometry is widely used for quantitative analysis due to its sensitivity, selectivity, accuracy and ease. Both absorbing and non-absorbing
UV-Visible Spectroscopy is a technique that uses light in the visible and adjacent ranges. It works based on absorption of light by molecules. Key points:
1. Absorption of light is based on electronic transitions in molecules. Different types of transitions (π-π*, n-π*) result in different absorption bands.
2. Chromophores and auxochromes determine the wavelength of absorption. Auxochromes cause bathochromic shifts.
3. Instruments use various components like light sources, monochromators and detectors to isolate wavelengths and measure absorption.
4. Factors like temperature, solvent and concentration affect the absorption spectrum based on Beer-Lambert law.
Spectral signatures are the specific combination of emitted, reflected or absorbed electromagnetic radiation (EM) at varying wavelengths which can uniquely identify an object. Here, i have focused on the spectral signature of water and the various micro-process that are responsible for it.
This document discusses infrared spectroscopy and the types of vibrations that can be observed using this technique. It provides an overview of the selection rules for infrared absorption and notes that vibrations that do not change the dipole moment of a molecule will not be observed. Typical absorption regions are highlighted, with the fingerprint region from 1300-400 cm-1 noted as providing information about the overall molecule. The effects of hydrogen bonding and common stretching frequencies for functional groups are summarized.
UV-visible spectroscopy involves using light in the UV-visible spectral region to analyze chemical substances. It works on the principle of Beer-Lambert's law, where absorbance is directly proportional to concentration and path length. Different functional groups and conjugated systems can absorb light at characteristic wavelengths. The technique is used for quantitative and qualitative analysis of samples through measurement of absorption spectra. It provides information about electronic transitions and molecular structure of compounds.
This document provides an overview of nuclear magnetic resonance (NMR) spectroscopy. It discusses the basic principles and instrumentation of NMR, solvent requirements, relaxation processes, chemical shifts and factors that affect chemical shifts. Common NMR solvents like CDCl3 and DMSO are described. Relaxation is explained as either spin-lattice (longitudinal) or spin-spin (transverse) processes. Chemical shifts result from shielding or deshielding of nuclei by electrons. Tetramethylsilane is used as an internal reference standard. Electronegativity, inductive effects, anisotropic effects, van der Waals deshielding and hydrogen bonding can influence chemical shifts.
Ultraviolet and visible spectroscopy is a technique that uses light in the UV-visible spectral region. It can be used to analyze organic molecules and determine their structure. Key concepts covered include electronic transitions, the Beer-Lambert law, and how solvents and conjugation affect UV-Vis spectra. UV-Vis spectroscopy can distinguish between isomers and functional groups, quantify substances, and identify unknown compounds.
Spectroscopic methods in inorganic chemistry Part1 uv visChris Sonntag
This document provides an overview of UV-Visible spectroscopy. It discusses electromagnetic radiation, the interaction of radiation with matter through electronic transitions, and terms used in UV-Visible spectroscopy like chromophores and auxochromes. It also describes concepts like wavelength and intensity shifts. Absorption of light can be influenced by conjugation, solvent effects, and functional groups. Finally, some applications of UV-Visible spectroscopy are mentioned, such as qualitative and quantitative analysis of compounds.
Ultrasound assisted reactions can enhance chemical synthesis through cavitation effects. Piezoelectric transducers are commonly used to generate ultrasound from 20 kHz to 2 MHz. Cavitation produces localized hot spots exceeding 4000K that can drive homogeneous and heterogeneous reactions. Homogeneous reactions involve single-phase systems and produce radicals from water sonolysis. Heterogeneous reactions involve multi-phase systems and benefit from improved mixing and mass transfer. Many reactions like esterification, hydrolysis, substitution, and addition have been achieved with higher yields and faster reaction times using ultrasound.
BASIC THEORY OF UV VISIBLE SPECTROSCOPY.pptxNittalVekaria
This document provides an overview of the basic theory of UV-visible spectroscopy. It discusses the origins of UV absorption and emission spectra from electronic transitions in molecules. The types of electronic transitions that can occur, such as n→π*, π→π*, and σ→σ* transitions, are explained. The effects of chromophores, auxochromes, and solvents are also summarized. Key concepts covered include electronic excitation and absorption, molecular orbitals, bonding and antibonding orbitals, and the factors that influence spectral peak positions.
This document discusses environmentally friendly synthetic strategies, specifically non-conventional methods like microwave irradiation and ultrasonication. It notes that these methods have advantages over conventional methods in being cleaner with higher yields and being more eco-friendly. The document outlines a strategy to synthesize new heterocyclic compounds by combining moieties like pyrazole, benzo-γ-pyrone, and quinoline, and studying the biological activity of the resulting products. It provides details on sonochemistry and microwave-assisted organic reactions, giving examples of reactions that can be performed using these techniques. The aims are to synthesize and characterize new heterocycles and evaluate their therapeutic potential, attempting the syntheses using both conventional and non-conventional
The document discusses UV spectroscopy and the different types of bands that can be observed. It explains that compounds with higher conjugation absorb at lower wavelengths due to a smaller energy gap between orbitals. Four main bands are described: K-band observed in conjugated double bonds with high intensity; R-band in carbonyl compounds with low intensity as it is a forbidden transition; B-band in aromatic/heteroaromatic compounds typically between 230-270nm; and E-band in benzenoid systems where benzene shows a strong band at 184nm.
There are four main types of shifts that can occur in the absorption maximum of compounds:
1. Bathochromic shift (Red shift) occurs when the absorption maximum shifts to longer wavelengths, such as when multiple chromophores are present in a molecule.
2. Hypsochromic shift (Blue shift) occurs when the absorption maximum shifts to shorter wavelengths, due to removal of conjugation or changes in solvent polarity.
3. Hyperchromic shift increases the intensity of absorption at the same wavelength maximum, often due to the introduction of auxochromes.
4. Hypochromic shift decreases the intensity of absorption, which can result from structural deformations introduced by certain groups.
This document discusses chromophores and how solvents affect absorption spectra. It defines a chromophore as a covalently bonded group that absorbs UV or visible radiation. Chromophores are classified as independent or dependent based on the number needed to impart color. Absorption maxima can shift to longer (bathochromic) or shorter (hypsochromic) wavelengths due to auxochromes or solvent changes. Solvent polarity also affects absorption based on the type of electronic transition involved. Temperature and solvent interactions determine the fineness of absorption bands.
Uv absorption spectra arise from electronic transitions in molecules where electrons move from lower to higher energy levels. The amount of energy absorbed is proportional to the concentration of the solution based on Beer-Lambert's law. Uv-visible spectroscopy can be used to determine structural information about organic compounds, identify additional impurities, and perform quantitative analysis of compounds that absorb uv radiation.
UV-Visible Spectroscopy involves studying the interaction of ultraviolet and visible light with molecules. When light of an appropriate wavelength is absorbed by a molecule, an electron is promoted to a higher energy orbital, exciting the molecule. The wavelength of absorbed light provides information about energy gaps related to functional groups. Absorption follows Beer's law - absorption is proportional to concentration and path length. Molar absorptivity values characterize absorption strength. Chromophores are the parts of molecules that absorb UV-visible light. Conjugation and substituent effects can cause shifts and changes in absorption intensity.
UV-Visible Spectroscopy involves the interaction of electromagnetic radiation in the ultraviolet and visible spectral regions with matter. When molecules absorb this radiation, electrons are excited from one energy level to a higher level. This causes absorption bands to appear in the absorption spectrum. Beer's law states that absorbance is directly proportional to concentration and path length. Chromophores are groups that absorb radiation, while auxochromes shift absorption to longer wavelengths by extending conjugation. Spectroscopy has applications in quantitative analysis, qualitative analysis, detection of functional groups and impurities, and determination of properties like extent of conjugation.
UV-Visible spectroscopy uses electromagnetic radiation to analyze molecular structure by measuring absorption of specific wavelengths. It follows Beer's and Lambert's laws, where absorbance is proportional to concentration. Absorption is due to electronic transitions between orbitals. Deviations from Beer's law can occur at high concentrations or due to chemical changes. Chromophores and auxochromes determine absorption wavelength. Applications include structure elucidation, quantitative analysis, and detection of impurities.
This document discusses ultraviolet-visible spectroscopy and its principles. It covers the electromagnetic spectrum, units used, absorption laws including Lambert's law and Beer's law. It describes chromophores and auxochromes, types of electronic transitions, factors affecting absorption bands, and solvent effects. Different types of absorption bands and applications of UV-Vis spectroscopy are also summarized.
1) The absorption of light by organic compounds involves the promotion of electrons from ground state to excited state molecular orbitals. Sigma electrons undergo σ-σ* transitions at shorter wavelengths while pi and non-bonding electrons undergo π-π* and n-π* transitions at longer wavelengths.
2) Chromophores are functional groups responsible for electronic transitions, imparting color. Auxochromes enhance absorption by chromophores through resonance. Conjugation and pH can shift absorption to longer wavelengths while dilution, solvents, and temperature can affect absorption spectra.
3) Spectrophotometry is widely used for quantitative analysis due to its sensitivity, selectivity, accuracy and ease. Both absorbing and non-absorbing
UV-Visible Spectroscopy is a technique that uses light in the visible and adjacent ranges. It works based on absorption of light by molecules. Key points:
1. Absorption of light is based on electronic transitions in molecules. Different types of transitions (π-π*, n-π*) result in different absorption bands.
2. Chromophores and auxochromes determine the wavelength of absorption. Auxochromes cause bathochromic shifts.
3. Instruments use various components like light sources, monochromators and detectors to isolate wavelengths and measure absorption.
4. Factors like temperature, solvent and concentration affect the absorption spectrum based on Beer-Lambert law.
Spectral signatures are the specific combination of emitted, reflected or absorbed electromagnetic radiation (EM) at varying wavelengths which can uniquely identify an object. Here, i have focused on the spectral signature of water and the various micro-process that are responsible for it.
This document discusses infrared spectroscopy and the types of vibrations that can be observed using this technique. It provides an overview of the selection rules for infrared absorption and notes that vibrations that do not change the dipole moment of a molecule will not be observed. Typical absorption regions are highlighted, with the fingerprint region from 1300-400 cm-1 noted as providing information about the overall molecule. The effects of hydrogen bonding and common stretching frequencies for functional groups are summarized.
UV-visible spectroscopy involves using light in the UV-visible spectral region to analyze chemical substances. It works on the principle of Beer-Lambert's law, where absorbance is directly proportional to concentration and path length. Different functional groups and conjugated systems can absorb light at characteristic wavelengths. The technique is used for quantitative and qualitative analysis of samples through measurement of absorption spectra. It provides information about electronic transitions and molecular structure of compounds.
This document provides an overview of nuclear magnetic resonance (NMR) spectroscopy. It discusses the basic principles and instrumentation of NMR, solvent requirements, relaxation processes, chemical shifts and factors that affect chemical shifts. Common NMR solvents like CDCl3 and DMSO are described. Relaxation is explained as either spin-lattice (longitudinal) or spin-spin (transverse) processes. Chemical shifts result from shielding or deshielding of nuclei by electrons. Tetramethylsilane is used as an internal reference standard. Electronegativity, inductive effects, anisotropic effects, van der Waals deshielding and hydrogen bonding can influence chemical shifts.
Ultraviolet and visible spectroscopy is a technique that uses light in the UV-visible spectral region. It can be used to analyze organic molecules and determine their structure. Key concepts covered include electronic transitions, the Beer-Lambert law, and how solvents and conjugation affect UV-Vis spectra. UV-Vis spectroscopy can distinguish between isomers and functional groups, quantify substances, and identify unknown compounds.
Spectroscopic methods in inorganic chemistry Part1 uv visChris Sonntag
This document provides an overview of UV-Visible spectroscopy. It discusses electromagnetic radiation, the interaction of radiation with matter through electronic transitions, and terms used in UV-Visible spectroscopy like chromophores and auxochromes. It also describes concepts like wavelength and intensity shifts. Absorption of light can be influenced by conjugation, solvent effects, and functional groups. Finally, some applications of UV-Visible spectroscopy are mentioned, such as qualitative and quantitative analysis of compounds.
Ultrasound assisted reactions can enhance chemical synthesis through cavitation effects. Piezoelectric transducers are commonly used to generate ultrasound from 20 kHz to 2 MHz. Cavitation produces localized hot spots exceeding 4000K that can drive homogeneous and heterogeneous reactions. Homogeneous reactions involve single-phase systems and produce radicals from water sonolysis. Heterogeneous reactions involve multi-phase systems and benefit from improved mixing and mass transfer. Many reactions like esterification, hydrolysis, substitution, and addition have been achieved with higher yields and faster reaction times using ultrasound.
BASIC THEORY OF UV VISIBLE SPECTROSCOPY.pptxNittalVekaria
This document provides an overview of the basic theory of UV-visible spectroscopy. It discusses the origins of UV absorption and emission spectra from electronic transitions in molecules. The types of electronic transitions that can occur, such as n→π*, π→π*, and σ→σ* transitions, are explained. The effects of chromophores, auxochromes, and solvents are also summarized. Key concepts covered include electronic excitation and absorption, molecular orbitals, bonding and antibonding orbitals, and the factors that influence spectral peak positions.
This document discusses environmentally friendly synthetic strategies, specifically non-conventional methods like microwave irradiation and ultrasonication. It notes that these methods have advantages over conventional methods in being cleaner with higher yields and being more eco-friendly. The document outlines a strategy to synthesize new heterocyclic compounds by combining moieties like pyrazole, benzo-γ-pyrone, and quinoline, and studying the biological activity of the resulting products. It provides details on sonochemistry and microwave-assisted organic reactions, giving examples of reactions that can be performed using these techniques. The aims are to synthesize and characterize new heterocycles and evaluate their therapeutic potential, attempting the syntheses using both conventional and non-conventional
The document discusses UV spectroscopy and the different types of bands that can be observed. It explains that compounds with higher conjugation absorb at lower wavelengths due to a smaller energy gap between orbitals. Four main bands are described: K-band observed in conjugated double bonds with high intensity; R-band in carbonyl compounds with low intensity as it is a forbidden transition; B-band in aromatic/heteroaromatic compounds typically between 230-270nm; and E-band in benzenoid systems where benzene shows a strong band at 184nm.
This document discusses ultraviolet-visible (UV-Vis) spectroscopy. It begins by defining spectroscopy and describing the electromagnetic radiation spectrum. It then focuses on UV-Vis spectroscopy, explaining that it involves electronic transitions in molecules caused by the absorption of ultraviolet or visible light. The major electronic transitions that can occur are defined, including σ → σ*, n → σ*, π → π*, and n → π* transitions. Factors that affect these transitions, such as conjugation, are also discussed. Real-world examples of molecular structures and the transitions they undergo are provided.
The document discusses various spectroscopic methods used in organic chemistry including UV-Visible, Infrared, Nuclear Magnetic Resonance, and Mass Spectroscopy. It explains the basic principles of spectroscopy such as how electromagnetic radiation interacts with molecules by absorption or emission of energy. The document also provides details on the instrumentation used in spectroscopy including spectrophotometers and spectrographs.
The document discusses green chemistry as a remedy for environmental pollution. It defines green chemistry as the generation of new products and processes that reduce or eliminate hazardous materials. The need for green chemistry is explained by new environmental problems, harmful side effects of some chemicals like DDT, and accidents. Advantages of green chemistry include being eco-friendly, energy efficient, producing less waste and safer products. The principles of green chemistry focus on preventing waste, improving atom economy in synthesis, using safer solvents and feedstocks, and designing for energy efficiency and degradation. Examples are given around safer chemical design and replacing hazardous solvents.
The document discusses chemistry problems and solutions presented by B.Sateesh Kumar, an assistant professor of chemistry at GDC(M)-SKLM. It includes 3 chemistry problems involving the products of reactions and Kumar's explanations of the major products formed. Specifically, it discusses hydrogenolysis to deprotect functional groups on amino acids, the reduction of an epoxide to an alcohol using LAH, and a two-step reaction sequence involving a Schmidt reaction and Boc protection.
DIBAL-H is a commercially available selective reducing agent that can reduce esters and nitriles to the corresponding aldehydes. It is prepared by heating triisobutylaluminum, which induces beta hydride elimination to form DIBAL-H and isobutene. DIBAL-H selectively reduces esters to aldehydes at low temperatures through a tetrahedral intermediate. Hydrolytic workup of this intermediate then yields the desired aldehyde products. The document provides an introduction to DIBAL-H including its preparation, applications in organic synthesis, and how it differs from other reducing agents like LiAlH4.
The document discusses sodium cyanoborohydride (NaBH3CN), including its preparation from sodium borohydride and hydrogen cyanide, properties such as being a less reactive reducing agent than sodium borohydride, solubility in solvents like THF and methanol, and ability to reduce protonated aldehydes and ketones at pH 3 but not neutral aldehydes and ketones. Main applications of sodium cyanoborohydride include its use as a reducing agent in organic synthesis reactions.
Strategies for Effective Upskilling is a presentation by Chinwendu Peace in a Your Skill Boost Masterclass organisation by the Excellence Foundation for South Sudan on 08th and 09th June 2024 from 1 PM to 3 PM on each day.
বাংলাদেশের অর্থনৈতিক সমীক্ষা ২০২৪ [Bangladesh Economic Review 2024 Bangla.pdf] কম্পিউটার , ট্যাব ও স্মার্ট ফোন ভার্সন সহ সম্পূর্ণ বাংলা ই-বুক বা pdf বই " সুচিপত্র ...বুকমার্ক মেনু 🔖 ও হাইপার লিংক মেনু 📝👆 যুক্ত ..
আমাদের সবার জন্য খুব খুব গুরুত্বপূর্ণ একটি বই ..বিসিএস, ব্যাংক, ইউনিভার্সিটি ভর্তি ও যে কোন প্রতিযোগিতা মূলক পরীক্ষার জন্য এর খুব ইম্পরট্যান্ট একটি বিষয় ...তাছাড়া বাংলাদেশের সাম্প্রতিক যে কোন ডাটা বা তথ্য এই বইতে পাবেন ...
তাই একজন নাগরিক হিসাবে এই তথ্য গুলো আপনার জানা প্রয়োজন ...।
বিসিএস ও ব্যাংক এর লিখিত পরীক্ষা ...+এছাড়া মাধ্যমিক ও উচ্চমাধ্যমিকের স্টুডেন্টদের জন্য অনেক কাজে আসবে ...
Thinking of getting a dog? Be aware that breeds like Pit Bulls, Rottweilers, and German Shepherds can be loyal and dangerous. Proper training and socialization are crucial to preventing aggressive behaviors. Ensure safety by understanding their needs and always supervising interactions. Stay safe, and enjoy your furry friends!
Macroeconomics- Movie Location
This will be used as part of your Personal Professional Portfolio once graded.
Objective:
Prepare a presentation or a paper using research, basic comparative analysis, data organization and application of economic information. You will make an informed assessment of an economic climate outside of the United States to accomplish an entertainment industry objective.
How to Build a Module in Odoo 17 Using the Scaffold MethodCeline George
Odoo provides an option for creating a module by using a single line command. By using this command the user can make a whole structure of a module. It is very easy for a beginner to make a module. There is no need to make each file manually. This slide will show how to create a module using the scaffold method.
How to Fix the Import Error in the Odoo 17Celine George
An import error occurs when a program fails to import a module or library, disrupting its execution. In languages like Python, this issue arises when the specified module cannot be found or accessed, hindering the program's functionality. Resolving import errors is crucial for maintaining smooth software operation and uninterrupted development processes.
it describes the bony anatomy including the femoral head , acetabulum, labrum . also discusses the capsule , ligaments . muscle that act on the hip joint and the range of motion are outlined. factors affecting hip joint stability and weight transmission through the joint are summarized.
The simplified electron and muon model, Oscillating Spacetime: The Foundation...RitikBhardwaj56
Discover the Simplified Electron and Muon Model: A New Wave-Based Approach to Understanding Particles delves into a groundbreaking theory that presents electrons and muons as rotating soliton waves within oscillating spacetime. Geared towards students, researchers, and science buffs, this book breaks down complex ideas into simple explanations. It covers topics such as electron waves, temporal dynamics, and the implications of this model on particle physics. With clear illustrations and easy-to-follow explanations, readers will gain a new outlook on the universe's fundamental nature.
A Strategic Approach: GenAI in EducationPeter Windle
Artificial Intelligence (AI) technologies such as Generative AI, Image Generators and Large Language Models have had a dramatic impact on teaching, learning and assessment over the past 18 months. The most immediate threat AI posed was to Academic Integrity with Higher Education Institutes (HEIs) focusing their efforts on combating the use of GenAI in assessment. Guidelines were developed for staff and students, policies put in place too. Innovative educators have forged paths in the use of Generative AI for teaching, learning and assessments leading to pockets of transformation springing up across HEIs, often with little or no top-down guidance, support or direction.
This Gasta posits a strategic approach to integrating AI into HEIs to prepare staff, students and the curriculum for an evolving world and workplace. We will highlight the advantages of working with these technologies beyond the realm of teaching, learning and assessment by considering prompt engineering skills, industry impact, curriculum changes, and the need for staff upskilling. In contrast, not engaging strategically with Generative AI poses risks, including falling behind peers, missed opportunities and failing to ensure our graduates remain employable. The rapid evolution of AI technologies necessitates a proactive and strategic approach if we are to remain relevant.
3. • Changes in chemical structure or the environment lead to
changes in the absorption spectrum of molecules and
materials
Bathochromic Shift : a shift of λmax towards lower energy or longer
wavelength (often called a red shift).
Hypsochromic Shift : a shift of λmax towards higher energy or shorter
wavelength (often called a blue shift)
Hyperchromic Shift : The shifting of molar absorptivity(absorption
intensity) towards higher values(increases).
Hypochromic shift : The shifting of molar absorptivity (absorption
intensity) towards lower values(decreases).
1
2
3
4
4. • Absorption maximum(λmax) shifted towards
longer wavelength.
Bathochromic shift
NH2
max
255 nm
max
280 nm
Benzene aniline
1
5. • Absorption maximum(λmax) shifted towards
shorter wavelength.
Hypsochromic shift
NH2
max
203 nm
max
280 nm
Anilinium ion
Aniline
NH3
H
2
6. • Absorption Intensity maximum(ɛmax) shifted
towards higher values.
Hyperchromic shift
N
N
max
3550
max
2550
2-methyl Pyridine
Pyridine
3
7. • Absorption Intensity maximum(ɛmax) shifted
towards lower values.
Hypochromic shift
max
10,500
max
19000
2-methyl biphenyl
biphenyl
4