Will Chlorine Fade Red Hair Dye?

Will chlorine fade red hair dye?

Will Chlorine Fade Red Hair Dye? 1

There are many factors you have to consider before you decide to go swimming. If when you shampoo your hair the color bleeds I would not go to the water park. Your hair fading should be your last thought, chlorine and dye are not friends. The chlorine could completely change the color of your hair. I would suggest using a swim cap or at least a bandana or head scarf to some what protect your hair and scalp. & be sure to completely rinse the chlorine out of your hair and give yourself a deep conditioning because the chlorine can damage your hair.

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what are the structural differences among chlorine atoms, chlorine molecules, and chloride ions?

Chlorine Atoms -- this is *one* chlorine so 17p, 17e, 18n Chlorine Molecules -- this is *two* chlorines covalently linked (share one pair of electrons) Cl-Cl Chloride Ion -- The chlorine atom has accepted one electron from an electrophile/metal/sodium 17p, 18e, 18n, negative one charge

Will Chlorine Fade Red Hair Dye? 2

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Will the chlorine affect my dyed hair?

the blonde will turn slightly greenish, yes. and chlorine is bad for your hair - damages it & dries it out. but if you wet your hair first, with clean tap water - your hair absorbs that water instead of the chlorinated water so it does not damage your hair or turn it green.

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My nails are so dry from the chlorine?

I am a competative swimmer too; and I've seen that with all my friends too. I am not in the water that long but, you can try lotion and massaging it every night before you go to bed; and a manicure once in a while should not hurt. I've noticed with green nail polish; after getting in the water it comes off too; but it leaves like a "yellow stain" on the nails. Maybe you are also using the wrong color. If nothing helps, consult your Doctor.

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What is the best type of filter to remove chlorine from my water?

Carbon filters are the most commonly used filter to remove chlorine from the water. The carbon media reduces the chlorine to chloride. I got a good filter from Isopurewater.com

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chlorine gas need specifics pleazz?

Its hard to tell because you dont give the ingrediants in the second substance, but i think i know. Its called a single replacement. The chlorine is chemically combined with something in one of the products. When the products are mixed together something in one product replaces chlorine so that chlorine then is alone out in the open as a gas.

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is chlorine ductile and malleable?

Ductility and malleability are properties that apply only to solids. They refer to ways something can be shaped by drawing or rolling or hammering. Chlorine is a gas and cannot be shaped. Therefore, it is neither ductile or malleable.

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How to minimize/ eliminate chlorine smell in a poolhouse?

very simple get an open bag of charcoal and stick it in there and it will absorb the smell or use open box of baking soda

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Why is more 2-chloropropane produced than 1-chloropropane in a reaction between propane and chlorine?

Observe a molecule of propane: CH_3CH_2CH_3. There are a total of six hydrogen atoms on the first carbon(s) while there are only two on the second carbon. This must mean that, if substitution was fair, you should get a product ratio between 1-chloropropane and 2-chloropropane a rough 3:1. However, the actual ratio is skewed towards the 2-chloropropane. Why?C_3H_8 Cl_2 xrightarrowtexthf C_3H_7Cl HClThe above reaction might look simple, but it actually has deceptively numerous steps involved. The first step is called initiation, where a photon (usually UV range) fissures the bond between the chlorine molecule (hence u2018initiationu2019, since it starts the process):Initiation: Cl_2 xrightarrowtexthf 2ClcdotBy doing so, you form two free radicals of chlorine, each with one unpaired electron. Now, free radicals are very reactive, so now you head on to the second step where it reacts with the propane molecule (this step is call propagation):Propagation: Clcdot C_3H_8 rightarrow cdotC_3H_7 HClThe above step is the important step. If you notice, there are three carbons, with two possible carbons (1st and 3rd are the same thing here, really) where the free radical can attach itself to. So, you have two possible arrangements of the carbocation:cdotCH_2CH_2CH_3 or CH_3dottextCHCH_3The funny thing to note is that due to hyperconjugation (an interaction between the sigma bond an adjacent empty p-orbital) the latter is more stable. Why is it more stable? You could see it in this way too. The carbocation has a positive charge, while the alkyl groups are electron donors (which are negatively charged). If you have more alkane groups surrounding a carbocation, it helps u2018cutu2019 down that positive charge. Carbocations | Image credit hereSince the secondary carbocation is more stable (due to greater amount of alkyl groups), it is more favoured in a reaction. As such, you see more of the latter than the former, and since they are in a transition state, reacts with the chlorine free radical to finally lead to our third step: termination.Termination: cdotC_3H_7 Clcdot rightarrow C_3H_7ClIn a summary, the secondary carbocation is more stable than the primary carbocation, hence it is more favoured in a reaction. As such, you are likely to form more of the former than the latter, giving a greater secondary haloalkane yield than primary.Why is more 2-chloropropane produced than 1-chloropropane in a reaction between propane and chlorine?Why is more 2-chloropropane than 1-chloropropane in a reaction between propane and chlorine?

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