endobj ��K0ށi���A����B�ZyCAP8�C���@��&�*���CP=�#t�]���� 4�}���a � ��ٰ;G���Dx����J�>���� ,�_“@��FX�DB�X$!k�"��E�����H�q���a���Y��bVa�bJ0՘c�VL�6f3����bձ�X'�?v 6��-�V`�`[����a�;���p~�\2n5��׌���� �&�x�*���s�b|!� Terminal alkynes form insoluble metal acetylides and precipate 13) Attack on the less sterically hindered primary bromide (bromoethane) is more favorable. {�%P �*�ª(w����';"N�i�+�h�c��HI^�N]��߅H���D�&�?��L�t�`cn�� ��^���(n���&�Ht0Xl��F�NKň�21 ,���X:�-_�9�TC���Y��K�I�M��S�=. Draw the line bond structures for the following alkenes, cyclic alkenes, and alkynes: a) noncyclic alkenes that contain 4 carbon atoms (3 possible) b) cyclic alkenes that contain 4 carbon atoms (4 possible) c) alkynes that contain 4 carbon atoms (2 possible, neither of them is a cyclic alkyne) 2. endobj << /Length 21 0 R /N 3 /Alternate /DeviceRGB /Filter /FlateDecode >> Alkenes and Alkynes Worksheet and Key 1. 2612 %��������� endobj Displaying top 8 worksheets found for - Alkanes And Alkenes. endobj << /Length 24 0 R /Filter /FlateDecode >> Displaying top 8 worksheets found for - Alkanes And Alkenes. 1) o hcl ch3oh 2) hcl ch3 3) hcl 4) hcl 5) hbr 6) hcl 7) ch3 h3o + 8) h3o + 9) h3o + 10) hg(oac)2, h2o nabh4 ch3 11) hg(oac)2, h2o nabh4. [ /ICCBased 20 0 R ] This interactive quiz and worksheet combo will test how much you know about the type of organic chemical compounds called alkynes. It would have to have two groups attached to show cis-trans isomerism. There is NO intermediate. 5 0 obj �FV>2 u�����/�_$\�B�Cv�< 5]�s.,4�&�y�Ux~xw-bEDCĻH����G��KwF�G�E�GME{E�EK�X,Y��F�Z� �={$vr����K���� Reaction of an alkynide with the secondary (hindered) bromide would result mostly in elimination instead of substitution. Groups that are trans on the alkene will end up trans on the cyclopropane product. {�KFE,��W5��eoY�WM���. Combustion Alkane + O 2 → CO 2 + H 2 O 2. stream Found worksheet you are looking for? stream A1�v�jp ԁz�N�6p\W� p�G@ Groups that are cis on the alkene will end up cis on the cyclopropane product. ��OE�S�K���A��ѻT6B�@�MM��\Τ7�{ǢO�M ���!�B�8Ẍ́��](^�NĂGGq�ˊK��c'�D���"Yz���k?��A����s�[m$Xt.����]Q�����R.��V��xZAA��Ф��``�lc���Q�ECW�Ea>XC����`��iʁ�uC�('�I�{��o� �k ��c!��y^ Acid-base reaction 2) 11) B 12) Add a solution of Cu+ or Ag+. /TT2 9 0 R /TT8 15 0 R /TT12 19 0 R /TT10 17 0 R /TT6 13 0 R >> >> E�6��S��2����)2�12� ��"�įl���+�ɘ�&�Y��4���Pޚ%ᣌ�\�%�g�|e�TI� ��(����L 0�_��&�l�2E�� ��9�r��9h� x�g��Ib�טi���f��S�b1+��M�xL����0��o�E%Ym�h�����Y��h����~S�=�z�U�&�ϞA��Y�l�/� �$Z����U �m@��O� � �ޜ��l^���'���ls�k.+�7���oʿ�9�����V;�?�#I3eE妧�KD����d�����9i���,�����UQ� ��h��6'~�khu_ }�9P�I�o= C#$n?z}�[1 x�Z;��6��+x����'-���ϸIg`�8�)�0��I�����"{�i�8��|�O��$�//�:��������3�j�^W��|�����Ҽu"���˸F6�ְ�P;��=x��+�E��'҂`�y��4l�4o��{�>�~z�j�.ة��7���������ǧQ�ɯ5�UMݝw? Alkenes and alkynes can be transformed into almost any other functional group you can name! 1637 Ⱦ�h���s�2z���\�n�LA"S���dr%�,�߄l��t� You can & download or print using the browser document reader options. alkene reactions and mechanisms for questions 1-24, give the major organic product of the reaction, paying particular attention to regio- and stereochemical outcomes. endstream Key Takeaway • Alkynes are hydrocarbons with carbon-to-carbon triple bonds and properties 4 0 obj 21 0 obj Some of the worksheets for this concept are Alkanes and alkenes work, Alkenes and alkynes work, Work naming and drawing alkanes, Work alkenes, Naming and drawing alkenes work and key, Chapter 8, Naming organic compounds alkanes, Chapter 1 organic compounds alkanes. endobj [7A�\�SwBOK/X/_�Q�>Q�����G�[��� �`�A�������a�a��c#����*�Z�;�8c�q��>�[&���I�I��MS���T`�ϴ�k�h&4�5�Ǣ��YY�F֠9�=�X���_,�,S-�,Y)YXm�����Ěk]c}džj�c�Φ�浭�-�v��};�]���N����"�&�1=�x����tv(��}�������'{'��I�ߝY�)� Σ��-r�q�r�.d.�_xp��Uە�Z���M׍�v�m���=����+K�G�ǔ����^���W�W����b�j�>:>�>�>�v��}/�a��v���������O8� � endstream << /ProcSet [ /PDF /Text ] /ColorSpace << /Cs1 7 0 R >> /Font << /TT4 11 0 R stream Alkenes have double bonds; alkynes have triple bonds. To download/print, click on pop-out icon or print icon to worksheet to print or download. endobj Cracking Cracking breakes a big molecule into smaller molecules. endobj 12) hg(oac)2, ch3oh nabh 4 13) ch3 bh3 thf 4-methyl-1-pentyne 3. Reactions of Alkanes 1. We will review their nomenclature, and also learn about the vast possibility of reactions using alkenes and alkynes as starting materials. 14) 20 0 obj 3/k��E�h�� ��s�H)+Ǣ��r0±[�hi �Y#�G�0���3FvafGH�/Ӫ�� ��.UŚ9��F��K!�%�˛�B�m�#CjS%|F�FV �1��>0Ǯ��׶�ӵ���̎�4���aׂ�C�d�b��Rñ���+��ē���3��+���� ���ӓ b~� U# &�Z���t]�,:F�����!n�+ٿ%���J�E�k"WG���cH_w�j�A������%�CX�_9˽����r䐵VRV��eį�}"7� No; a triply bonded carbon atom can form only one other bond. 2. %PDF-1.3 About This Quiz & Worksheet. The cyclopropanation reaction of an alkene with a carbene takes place in a single step. Worksheet will open in a new window. O*��?�����f�����`ϳ�g���C/����O�ϩ�+F�F�G�Gό���z����ˌ��ㅿ)����ѫ�~w��gb���k��?Jި�9���m�d���wi獵�ޫ�?�����c�Ǒ��O�O���?w| ��x&mf������ Substitution Reaction Reaction by a halogen in presence of UV light. << /Length 5 0 R /Filter /FlateDecode >> >> ߏƿ'� Zk�!� $l$T����4Q��Ot"�y�\b)���A�I&N�I�$R$)���TIj"]&=&�!��:dGrY@^O�$� _%�?P�(&OJEB�N9J�@y@yC�R �n�X����ZO�D}J}/G�3���ɭ���k��{%O�חw�_.�'_!J����Q�@�S���V�F��=�IE���b�b�b�b��5�Q%�����O�@��%�!BӥyҸ�M�:�e�0G7��ӓ����� e%e[�(����R�0`�3R��������4�����6�i^��)��*n*|�"�f����LUo�՝�m�O�0j&jaj�j��.��ϧ�w�ϝ_4����갺�z��j���=���U�4�5�n�ɚ��4ǴhZ�Z�Z�^0����Tf%��9�����-�>�ݫ=�c��Xg�N��]�. 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