Chemistry, asked by suchianjali307, 7 months ago

In the mass spectrum of toluene, strong peaks are formed at m/e 91 an m/e 65.

Also a broad peak appear at 46.4. Justify the origin of these signals .

Answers

Answered by laxmitomar1983
0

An invaluable tool in organic structure determination and verification involves the class of electromagnetic (EM) radiation with frequencies between 4000 and 400 cm-1 (wavenumbers). The category of EM radiation is termed infrared (IR) radiation, and its application to organic chemistry known as IR spectroscopy. Radiation in this region can be utilized in organic structure determination by making use of the fact that it is absorbed by interatomic bonds in organic compounds. Chemical bonds in different environments will absorb varying intensities and at varying frequencies. Thus IR spectroscopy involves collecting absorption information and analyzing it in the form of a spectrum -- The frequencies at which there are absorptions of IR radiation ("peaks" or "signals") can be correlated directly to bonds within the compound in question.

An invaluable tool in organic structure determination and verification involves the class of electromagnetic (EM) radiation with frequencies between 4000 and 400 cm-1 (wavenumbers). The category of EM radiation is termed infrared (IR) radiation, and its application to organic chemistry known as IR spectroscopy. Radiation in this region can be utilized in organic structure determination by making use of the fact that it is absorbed by interatomic bonds in organic compounds. Chemical bonds in different environments will absorb varying intensities and at varying frequencies. Thus IR spectroscopy involves collecting absorption information and analyzing it in the form of a spectrum -- The frequencies at which there are absorptions of IR radiation ("peaks" or "signals") can be correlated directly to bonds within the compound in question.An Example IR Spectrum

An invaluable tool in organic structure determination and verification involves the class of electromagnetic (EM) radiation with frequencies between 4000 and 400 cm-1 (wavenumbers). The category of EM radiation is termed infrared (IR) radiation, and its application to organic chemistry known as IR spectroscopy. Radiation in this region can be utilized in organic structure determination by making use of the fact that it is absorbed by interatomic bonds in organic compounds. Chemical bonds in different environments will absorb varying intensities and at varying frequencies. Thus IR spectroscopy involves collecting absorption information and analyzing it in the form of a spectrum -- The frequencies at which there are absorptions of IR radiation ("peaks" or "signals") can be correlated directly to bonds within the compound in question.An Example IR SpectrumBecause each interatomic bond may vibrate in several different motions (stretching or bending), individual bonds may absorb at more than one IR frequency. Stretching absorptions usually produce stronger peaks than bending, however the weaker bending absorptions can be useful in differentiating similar types of bonds (e.g. aromatic substitution). It is also important to note that symmetrical vibrations do not cause absorption of IR radiation. For example, neither of the carbon-carbon bonds in ethene or ethyne absorb IR radiation.

Please mark me as brainliest!

Attachments:
Similar questions