How To Locate Cell Phone

-

How To Locate Cell Phone


Cell phones have advanced quite a bit from the huge analog brick phones that people were sporting in the 80's. They are no longer just communication devices. There are several ways to use cell phones. One of them is a tracking device. You can locate cell phone with some simple technology Have a question? Get an answer from Online Tech Support now!

Instructions


  • You must have a modern phone to locate cell phone. One like the iphone or another smart phone.
  • Install a software program on the phone called Google Latitude.
  • Sign up for a Google account and set up Google maps.
  • To locate cell phone, you must have the application installed and activated on each phone you wish to be able to locate. Follow the above instructions for each phone you wish to use.
  • You can also install Google Maps on your computer to locate cell phone from your computer. You'll need a Google account for this as well. If you don't have one, it's free and easy to sign up.
  • Each person who you wish to use the software to locate cell phone must have the other person in their friends list. They must also give permission to the other users to be able to locate them. Users can give or restrict permission to anyone at anytime. Break up with your boyfriend? No problem. Just remove them from the list of people who can locate you with your cell phone.



Comments

Post a Comment

Popular posts from this blog

What Is Melting Points

-
Image
Most organic compounds have melting points below 200 ºC. Some decompose before melting, a few sublime, but a majority undergo repeated melting and crystallization without any change in molecular structure. When a pure crystalline compound is heated, or a liquid cooled, the change in sample temperature with time is roughly uniform. However, if the solid melts, or the liquid freezes, a discontinuity occurs and the temperature of the sample remains constant until the phase change is complete. This behavior is shown in the diagram on the right, with the green segment representing the solid phase, light blue the liquid, and red the temperature invariant liquid/solid equilibrium. For a given compound, this temperature represents its melting point (or freezing point), and is a reproducible constant as long as the external pressure does not change. The length of the horizontal portion depends on the size of the sample, since a quantity of heat proportional to the heat of fusion must be...
Read more

What Is Atomic And Molecular Orbitals

-
Image
A more detailed model of covalent bonding requires a consideration of valence shell atomic orbitals. For second period elements such as carbon, nitrogen and oxygen, these orbitals have been designated 2 s , 2p x , 2p y   & 2p z . The spatial distribution of electrons occupying each of these orbitals is shown in the diagram below.   Very nice displays of orbitals may be found at the following sites: J. Gutow, Univ. Wisconsin Oshkosh R. Spinney, Ohio State  M. Winter, Sheffield University The valence shell electron configuration of carbon is 2 s 2 , 2p x 1 , 2p y 1  & 2p z 0 . If this were the configuration used in covalent bonding, carbon would only be able to form two bonds. In this case, the valence shell would have six electrons- two shy of an octet. However, the tetrahedral structures of methane and carbon tetrachloride demonstrate that carbon can form four equivalent bonds, leading to the desired octet. In order to explain this covalent bonding,...
Read more

Uses OF Alkynes In Nature And Medicine

-
Alkynes in nature and medicine According to Ferdinand Bohlmann, the first naturally occurring acetylenic compound, dehydromatricaria ester, was isolated from an Artemisia  species in 1826 . Polyynes, a subset of this class of natural products, have been isolated from a wide variety of plant species, cultures of higher fungi, bacteria, marine sponges, and corals.  Some acids like  tariric acid  contains an alkyne group. Diynes and triynes, species with the linkage RC ≡ C-C ≡ CR' and RC ≡ C-C ≡ C-C ≡ CR' respectively, occur in certain plants ( Ichthyothere , Chrysanthemum ,  Cicuta ,  Oenanthe  and other members of the  Asteraceae  and  Apiaceae  families).  Some examples are  cicutoxin , oenanthotoxin ,  falcarinol  and  carotatoxin . These compounds are highly bioactive, e.g. as  nematocides .  1-Phenylhepta-1,3,5-triyne is illustrative of a naturally occurring triyne. Alkynes occ...
Read more