Special topic Conjugated, UV, & Woodward Feiser Flashcards

To pass because I will cry

1
Q

What happens when electron moves to a higher energy level

A

the attraction of the nucleus on electrons decreases. the electrons are freer and have more kinetic energy

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2
Q

The _____________ of ultraviolet (UV) light can promote an electron from a lower electronic state to a higher one

A

absorption

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3
Q

Ultraviolet light has a slightly _____________ wavelength (and, thus, _________frequency) than visible light

A

shorter,
higher

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4
Q

The most useful region of UV light for this purpose is ________________-.

A

200–400 nm

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5
Q

When electrons in a lower energy state (_____________) absorb light having the appropriate energy, an electron is promoted to a higher electronic state (_______________).

A

the ground state,
the excited state

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6
Q

The energy difference between the two states depends on the ________________.

A

location of the electron

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7
Q

The promotion of electrons in σ bonds and unconjugated π bonds requires light having a wavelength of _______________

A

LESS THAN 200 nm
< 200 nm

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8
Q

The light that is required for the promotion σ bonds and unconjugated π bonds has a less than 200 nm wavelength which means that, it has a _______ wavelength and ________ energy than light in the _______ region of the electro magnetic spectrum

A

shorter
higher
UV

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9
Q

With ____________, however, the energy difference between the ground and excited states ____________, so longer wavelengths of light can be used to promote electrons.

A

conjugated dienes
decreases

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10
Q

Why can we promote electrons with light which has longer wavelengths?

A

because with conjugated dienes the energy difference between the ground and excited states decreases

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11
Q

It is referred to as The wavelength of UV light absorbed by a compound.

A

λmax.

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12
Q

What is λmax.

A

It is referred to as The wavelength of UV light absorbed by a compound.

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13
Q

What wavelength does 1,3-Butadiene

A

It absorbs UV light at λmax = 217 nm

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14
Q

What wavelength does 1,3-cyclohexadiene

A

It absorbs UV light λmax of 256 nm

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15
Q

Which compound absorbs 217 nm and 256 nm? Which has higher energy?

A

1,3-Butadiene: 217 nm

1,3-cyclohexadiene: 256 nm

1,3-Butadiene has higher energy because it has a shorter wavelength

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16
Q

Arrange all the electromagnetic light in increasing energy.

A

Radio< Microwave< Infrared< Visible light< Ultra Violet< X-rays< Gamma rays

The shorter the wavelength the higher the energy

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17
Q

___________________ absorb light in the UV region of the electromagnetic spectrum (200–400 nm).

A

Conjugated dienes and polyenes

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18
Q

What causes the decrease in the energy difference between the ground state and excited state?

A

The increase of the number of conjugated π bonds.

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19
Q

What is the relationship of Energy and the number of conjugated π bonds?

A

Inversely proportional

20
Q

As the number of conjugated π bonds increases, the energy difference between the ground and excited state ___________, shifting the absorption to longer wavelengths.

A

decreases

21
Q

The absorption of longer wavelengths was caused by the ___________________.

A

Increase of the number of conjugated π bonds

and the decrease in energy difference between the ground and excited state

22
Q

How many conjugated π bonds does a molecule have when the absorption shifts from UV to Visible region?

A

Eight or more

23
Q

When it shifts from UV to visible does it absorb?

A

It does not absorb

24
Q

What wavelength from the visible region does Lycopene absorbs?

A

absorbs visible light at λmax = 470 nm

25
Q

What color does the 470 nm in the visible region falls?

A

blue-green region

26
Q

Why lycopene appears as red?

A

Because it does not absorb light in the red region, lycopene appears bright red.

27
Q

What does SPF stands for?

A

Sun Protection Factor

28
Q

Ultraviolet radiation from the sun is high enough in energy to _____________

A

cleave bonds

29
Q

These are formed by the cleaved bonds

A

radicals

30
Q

Radicals formed from cleave bonds can _______________.

A

prematurely age skin and cause skin cancers

31
Q

The ultraviolet region is often __________, based on the wavelength of UV light.

A

subdivided

32
Q

Wavelength range for UV-B

A

UV-B (290–320 nm)

33
Q

Wavelength range for UV-A

A

UV-A (320–400 nm)

34
Q

Wavelength range for UV-C

A

UV-C (< 290 nm)
LESS THAN 290 nm

35
Q

Which has UV variation is more dangerous?

A

UV-C because it’s wavelength is < 290 nm. It has the smallest wavelength among the 3 and because of its short wavelength, it has a higher energy compared to others.

36
Q

The highest energy UV light (UV-C) is filtered out by the _________.

A

ozone layer

37
Q

Only UV light having wavelengths ___________ reaches the skin’s surface.

A

greater than 290 nm (> 290 nm)

38
Q

Most of the UV light that reaches our skin are absorbed by ____________.

A

melanin

39
Q

What is melanin?

A

It is the highly conjugated colored pigment in the skin that serves as the body’s natural protection against the harmful effects of UV radiation.

40
Q

Prolonged exposure to the sun can _______________________ ___________________________.

A

allow more UV radiation to reach your skin than melanin can absorb.

41
Q

What is in the commercial sunscreens that offers added protection from the sun?

A

conjugated compounds that absorb UV light that shields your skin from the harmful effects of UV radiation.

42
Q

What are the 2 most common conjugated compounds used in sunscreens?

A

para-aminobenzoic acid (PABA) and padimate O.

43
Q

Conjugated compounds shield the skin from what variation of UV? UV-A, UV-B, or UV-C?

A

UV-B

44
Q

Conjugated compounds have often little effect on __________.

A

UV-A

45
Q

It does not burn the skin however it can still cause long-term damage to skin cells.

A

UV-A

46
Q

What are unsaturated hydrocarbons?

A

Unsaturated hydrocarbons are compounds composed of carbon and hydrogen atoms, with one or more carbon carbon double or triple bonds in their chemical structure

47
Q

What are conjugated compounds?

A

Conjugated dienes have the two double bonds separated by a single bond.

Conjugated compounds are molecules where alternating single and double bonds occur.