6 Organic Analysis Flashcards

(14 cards)

1
Q

high resolution mass spec

A

very sensitive so allows masses to be given to 4 or 5 d.p. . This is useful for compounds with the same Mr such as CH3CH2CH3 and CH3CHO

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2
Q

test for primary or secondary alcohols

A

use acidified potassium dichromate
goes from orange to green

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3
Q

test for aldehydes

A

Tollen’s Reagent - silver mirror formed
Fehling’s solution - brick red ppt formed from blue

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4
Q

test for alkenes

A

add bromine water
goes from orange to colourless

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5
Q

test for carboxylic acid

A

add sodium carbonate
produces CO2, which turns limewater cloudy

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6
Q

test for halolakanes

A

add NaOH and warm. Acidify using HNO3 and add AgNO3.
forms coloured precipitate of AgX

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7
Q

Mass spectrometry using time of flight

A

gives the Mr of the comounds

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8
Q

Why is electron impact a bad method to use with organic samples?

A

the sample can be fragmented, causing other, incorrect, peaks

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9
Q

how does infrared spectroscopy work?

A

bonds in the molecule absorb infrared radiation at characteristic wavelengths. The spectrometer measures the percent of infrared transmitted and produces a graph.

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10
Q

fingerprint region

A

area below 1500cm-1
unique for every compound and can be distinguished using known spectra from a data base

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11
Q

C=O infrared spectra

A

strong, sharp peak at 1680-1750 cm-1

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12
Q

O-H in alcohols infrared spectra

A

wide peak at 3230-3550 cm-1
wider due to hydrogen bonding

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13
Q

O-H in acids infrared spectra

A

very wide peak at 2500–3000 cm-1 due to delocalisation in the -COOH and hydrogen bonding

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14
Q

why does increase emissions of CH4, CO2, H2O etc cause an enhanced greenhouse effect?

A

they absorb infrared radiation in their bonds, retaining more heat, enhancing the greenhouse effect

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