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  2. 15 Ways to Repel Bugs Naturally (and Cheaply) - AOL

    www.aol.com/finance/15-ways-repel-bugs-naturally...

    Aside from the gratification of concocting DIY bug repellent, there's the benefit of its chemical-free composition. Ingredients needed for a bug-repellent lotion bar include coconut oil; shea ...

  3. How to make your own bug repellant in a cute mason jar - AOL

    www.aol.com/lifestyle/2016-06-07-how-to-make...

    Learn how to make your own mosquito repellant at home! With this fun DIY bug repellant in a mason jar, you won't be bored and you won't get bitten!

  4. Flea treatments - Wikipedia

    en.wikipedia.org/wiki/Flea_treatments

    Flea adults, larvae, or eggs can be controlled with insecticides. Lufenuron is a veterinary preparation (known as Program) that attacks the larval flea's ability to produce chitin, necessary for the adult's hard exoskeleton, but it does not kill fleas. Flea medicines need to be used with care because many of them also affect mammals.

  5. You Can Use Vinegar and Baking Soda To Remove Rust - AOL

    www.aol.com/lifestyle/vinegar-baking-soda-remove...

    The baking soda will neutralize the acidity of the solution, reducing its corrosive properties. Let it soak for 10 to 15 minutes. Thoroughly dry the object to prevent any future rust formation.

  6. Insect repellent - Wikipedia

    en.wikipedia.org/wiki/Insect_repellent

    Synthetic repellents tend to be more effective and/or longer lasting than "natural" repellents. [1] [2]For protection against ticks and mosquito bites, the U.S. Centers for Disease Control (CDC) recommends DEET, icaridin (picaridin, KBR 3023), oil of lemon eucalyptus (OLE), para-menthane-diol (PMD), IR3535 and 2-undecanone with the caveat that higher percentages of the active ingredient ...

  7. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

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